Polso SpO2 Accuracy Validation Study

The purpose of this study is to validate the SpO2 accuracy and performance of the Polso
Monitoring System during non-motion conditions over the range of 70-100% SaO2 as compared to
arterial blood samples assessed by CO-Oximetry for SpO2 validation. It is expected that the
Accuracy Root Mean Square (Arms) performance of the Polso Monitoring System will meet a
specification of 3.5% or less in non-motion conditions for the range of 70-100% SaO2 thereby
demonstrating an acceptable SpO2 accuracy performance specification.

The Control Pulse Oximeter, an FDA cleared device, is used to monitor the oxygen saturation
levels real time throughout the study for subject safety and to target stable plateaus. This
device is used to assess the stability of the data.

A whole blood analyzer (CO-Oximeter) is used as the reference standard device for obtaining
the functional SaO2 value from arterial blood samples obtained during the study.

A minimum of 10 healthy adult subjects, ranging in pigmentation from light to dark, will be
enrolled in the study to meet the study design requirements defined by ISO 80601-2-61:2011
and by the FDA's Guidance for Pulse Oximeters. The subjects will have an arterial catheter
placed in the radial artery to allow for simultaneous blood samples during stable plateaus of
induced hypoxic levels.

The study population will include 10-15 healthy non-smoking (or has refrained from smoking
for 2 days) competent adults 18-50 years of age. The subject selection will be an equitable
distribution of males and females of any race with varying skin tones including at least 2
darkly pigmented subjects or 15% of the subject pool, whichever is larger. Data collection
will occur over a 2-5 day period for this study population.

Inclusion Criteria:

- 10-15 Adults with a minimum of 4 males and a minimum of 4 females, with the balance
made up of either

- Subject must have the ability to understand and provide written informed consent

- Subject is 18 to 50 years of age

- Subject must be willing and able to comply with study procedures and duration

- Subject is a non-smoker or who has not smoked within 2 days prior to the study

Exclusion Criteria:

- Subject is considered as being morbidly obese (defined as BMI >39.5)

- Compromised circulation, injury, or physical malformation of fingers, wrist, hands,
ears or forehead/skull or other sensor sites which would limit the ability to test
sites needed for the study. (Note: Certain malformations may still allow subjects to
participate if the condition is noted and would not affect the particular sites
utilized.)

- Females who are pregnant, who are trying to get pregnant, or have a urine test
positive for pregnancy on the day of the study

- Smoker Subjects who have refrained will be screened for COHb levels >3% as assessed
with a Masimo Radical 7 (Rainbow)

- Subjects with known respiratory conditions such as: (self-reported)

- uncontrolled / severe asthma,

- flu,

- pneumonia / bronchitis,

- shortness of breath / respiratory distress,

- unresolved respiratory or lung surgery with continued indications of health
issues ,

- emphysema, COPD, lung disease

- Subjects with known heart or cardiovascular conditions such as: (self-reported, except
for blood pressure and ECG review)

- hypertension: systolic >140mmHg, Diastolic >90mmHg on 3 consecutive readings
(reviewed during health screen).

- have had cardiovascular surgery

- Chest pain (angina)

- heart rhythms other than a normal sinus rhythm or with respiratory sinus
arrhythmia (reviewed during health screen)

- previous heart attack

- blocked artery

- unexplained shortness of breath

- congestive heart failure (CHF)

- history of stroke

- transient ischemic attack

- carotid artery disease

- myocardial ischemia

- myocardial infarction

- cardiomyopathy

- Self-reported health conditions as identified in the Health Assessment Form
(self-reported)

- diabetes,

- uncontrolled thyroid disease,

- kidney disease / chronic renal impairment,

- history of seizures (except childhood febrile seizures),

- epilepsy,

- history of unexplained syncope,

- recent history of frequent migraine headaches,

- recent symptomatic head injury (within the last 2 months)

- cancer / chemotherapy

- Subjects with known clotting disorders (self-reported)

- history of bleeding disorders or personal history of prolonged bleeding from
injury

- history of blood clots

- hemophilia

- current use of blood thinner: prescription or daily use of aspirin

- Subjects with severe contact allergies to standard adhesives, latex or other materials
found in pulse oximetry sensors, ECG electrodes, respiration monitor electrodes or
other medical sensors (self-reported)

- Subjects with severe allergies to iodine (only applicable if iodine or similar is
used)

- Subjects with severe allergies lidocaine (or similar pharmacological agents, e.g.
Novocaine)

- Failure of the Perfusion Index Ulnar/Ulnar+Radial Ratio test (Ratio < 0.4)

- Unwillingness or inability to remove colored nail polish from test digits.

- Other known health condition, should be considered upon disclosure in health
assessment form