Accuracy Validation of Belun Oxygen Saturation Pulse Oximeter FDA Submission Study

The purpose of this study is to evaluate the SpO2 accuracy performance of Belun Ring Oximeter
placed on the index fingers during non-motion conditions over the range of 70-100% SaO2,
arterial blood samples, assessed by CO-Oximetry. It is expected that the Accuracy Root Mean
Square (ARMS) performance of the oximetry system will meet the required specification of ARMS
of 3.5% or less allowed for reflectance technology in non-motion conditions for the range of
70 - 100% SaO2.

The Clinimark proprietary Desaturation Fixture with Automated Data Collection is a single
limb blow by system used to deliver medical grade oxygen and nitrogen gas mixtures to induce
various hypoxic levels in subjects at a slow steady rate allowing an automatic marking and
collection of the Control or secondary Transfer reference Pulse Oximeter and other pulse
oximetry systems at 1 second intervals.

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.

Multi-parameter monitor used during the study to observe a subject's vital signs including
ECG tracing, heart rate, respiratory rate, end-tidal CO2 with capnograph, secondary monitor
for the oxygen concentration being delivered to the subject.

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.

Inclusion Criteria:

- 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.

- Male or female of any race.

- Subject demographics include a range of skin pigmentations, including at least 2
darkly pigmented subjects or 15% of the subject pool, whichever is larger.

Exclusion Criteria:

- Subject is considered as being morbidly obese (defined as BMI large than 39.5).

- Compromised circulation, injury, or physical malformation of fingers, toes, 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.

- Subjects with COHb levels larger than 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, respiratory or lung surgery, emphysema, COPD, lung disease.

- Subjects with known heart or cardiovascular conditions such as: (self-reported),
except for blood pressure and ECG review) hypertension, have had cardiovascular
surgery, Chest pain (angina), heart rhythms other than a normal sinus rhythm or with
respiratory sinus arrhythmia, 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, 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 head
injury, 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).

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

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