(337 days)
Not Found
No
The description details standard pulse oximetry technology based on light absorption and empirical formulas, with no mention of AI or ML algorithms for data processing or interpretation.
No.
The device is for spot-checking oxygen saturation and pulse rate, which are diagnostic measurements, not therapeutic interventions.
Yes
The device measures oxygen saturation and pulse rate, which are physiological parameters used to assess a patient's condition and help in the diagnosis and monitoring of various medical conditions. The "Intended Use / Indications for Use" states it is "intended for spot-checking oxygen saturation and pulse rate."
No
The device description explicitly states that the pulse oximeter consists of "probe, electronic circuits, and display and plastic enclosures," indicating it is a hardware device with embedded software, not a software-only medical device.
Based on the provided information, this device is not an IVD (In Vitro Diagnostic).
Here's why:
- IVD Definition: In vitro diagnostics are tests performed on samples taken from the human body, such as blood, urine, or tissue, to detect diseases, conditions, or infections. They are used to diagnose, monitor, or screen for health issues.
- Device Function: The description clearly states that the device is a pulse oximeter that measures oxygen saturation and pulse rate by placing a sensor on the finger. This is a non-invasive measurement taken directly from the body, not a test performed on a sample in vitro (outside the body).
- Measurement Principle: The description details the use of light absorption through the finger to determine oxygen saturation. This is a physical measurement, not a chemical or biological analysis of a sample.
Therefore, while this is a medical device used for diagnostic purposes (spot-checking oxygen saturation and pulse rate), it does not fit the definition of an In Vitro Diagnostic device.
N/A
Intended Use / Indications for Use
The Pulse Oximeter is intended for spot-checking oxygen saturation and pulse rate, and the device is a reusable device and intended to be used with the finger of adults in professional healthcare facility or home conditions when physician follow-up and operated by a physician. And it is not intended to be used under motion.
Product codes
DQA
Device Description
The pulse oximeter, Model OHT60 and OXH78, consists of probe, electronic circuits, and display and plastic enclosures, is designed for spot checking of the pulse oxygen saturation and pulse rate for adults in a professional healthcare facility or home conditions when physician follow-up and operated by a physician. This medical device can be reused. Not for continuously monitoring.
SpO2 is based on the absorption of pulse blood oxygen to red and infrared light by means of finger sensor and SpO2 measuring unit. The measurement principle of Pulse oximeter is based on the absorption spectrum characteristics of hemoglobin and oxyhemoglobin in red and infrared regions, and the empirical formula of data is established by using ' Lambert Beer ' law. The working principle of the instrument adopts photoelectric blood oxygen detection technology combined with volume pulse recording technology, The specific process is as follows: Firstly, the infrared light emitting at 660 nm and the near-infrared light emitting at 905 are used to irradiate the finger and the measurement data are obtained by the infrared receiver tube. Secondly, the obtained measurement data were calculated and processed by electronic circuits and microprocessors to obtain the blood oxygen saturation and pulse rate, and the calculation results were displayed on the screen.
The subject device is a reusable device, and need to reprocess as suggested in the user manual after each use. And the device is intended to be used on the finger, and powered by 2*1.5V AAA alkaline batteries.
The Model OHT60 and OXH78 have the same critical components and its materials and means of power supply, PCB layout and Software are little different.
Mentions image processing
Not Found
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
Not Found
Anatomical Site
finger
Indicated Patient Age Range
adults
Intended User / Care Setting
professional healthcare facility or home conditions when physician follow-up and operated by a physician.
Description of the training set, sample size, data source, and annotation protocol
Not Found
Description of the test set, sample size, data source, and annotation protocol
Clinical studies were conducted at Sir Run Run Shaw Hospital, School of Medicine, Zhejiang University to verify the accuracy of the subject device. The clinical study was conducted in accordance to ISO80601-2-61:2017, ISO14155:2020, and the FDA Guidance Document for Pulse Oximeters. The subject device of this study was to verify the accuracy of pulse oximetry (SpO2) measured by the oximeter with a measurement range of 70-100% in the static state.
The induced Fraction of inspiration O2 (FiO2) control test was performed on subjects, and the subjects were subjected to radial artery puncture and indwelling catheter to obtain a stable arterial blood sample. The pulse oxygen saturation (SpO2) measured by the oximeter is compared with the functional oxygen saturation (SaO2) in arterial blood is analyzed by the arterial blood gas analyzer(CO-OXIMETER).
12 healthy adult volunteer subjects (ages 21-42yr, 46-75kg, 150-180cm, with light to dark pigmentation) were included in the study conducted to evaluate and complete the SpO2 accuracy performance of the Pulse Oximeter. 4 males and 8 females (including 4 subjects with Fitzpatrick V, VI, 8 subjects with Fitzpatrick I ~ Fitzpatrick IV).
Summary of Performance Studies (study type, sample size, AUC, MRMC, standalone performance, key results)
Clinical studies were conducted at Sir Run Run Shaw Hospital, School of Medicine, Zhejiang University to verify the accuracy of the subject device.
The clinical study was conducted in accordance to ISO80601-2-61:2017, ISO14155:2020, and the FDA Guidance Document for Pulse Oximeters.
The subject device of this study was to verify the accuracy of pulse oximetry (SpO2) measured by the oximeter with a measurement range of 70-100% in the static state.
The measure result between the SpO2 measured by subject device and the SaO2 measured by the blood gas analyzer.
The SpO2 accuracy performance results showed the subject Pulse Oximeter to have an ARMS of 1.98 during steady state conditions over the range of 70-100%.
Sample size: 12 healthy adult volunteer subjects.
Key Metrics (Sensitivity, Specificity, PPV, NPV, etc.)
ARMS: 1.98 (for SpO2 accuracy)
Predicate Device(s)
Reference Device(s)
Not Found
Predetermined Change Control Plan (PCCP) - All Relevant Information
Not Found
§ 870.2700 Oximeter.
(a)
Identification. An oximeter is a device used to transmit radiation at a known wavelength(s) through blood and to measure the blood oxygen saturation based on the amount of reflected or scattered radiation. It may be used alone or in conjunction with a fiberoptic oximeter catheter.(b)
Classification. Class II (performance standards).
0
Image /page/0/Picture/0 description: The image contains the logo of the U.S. Food and Drug Administration (FDA). On the left is the Department of Health & Human Services logo. To the right of that is the FDA logo, which is a blue square with the letters "FDA" in white. To the right of the blue square is the text "U.S. FOOD & DRUG ADMINISTRATION" in blue.
January 4, 2024
Cofoe Medical Technology Co., Ltd. % Boyle Wang Official Correspondent Shanghai Truthful Information Technology Co., Ltd. RM.1801,No.161,East Lujiazui Rd.,Pudong Shanghai. Shanghai 200120 China
Re: K230277
Trade/Device Name: Pulse Oximeter(Model OHT60,OXH78) Regulation Number: 21 CFR 870.2700 Regulation Name: Oximeter Regulatory Class: Class II Product Code: DQA Dated: November 30, 2023 Received: December 4, 2023
Dear Boyle Wang:
We have reviewed your section 510(k) premarket notification of intent to market the device referenced above and have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate commerce prior to May 28, 1976, the enactment date of the Medical Device Amendments, or to devices that have been reclassified in accordance with the provisions of the Federal Food, Drug, and Cosmetic Act (the Act) that do not require approval of a premarket approval application (PMA). You may, therefore, market the device, subject to the general controls provisions of the Act. Although this letter refers to your product as a device, please be aware that some cleared products may instead be combination products. The 510(k) Premarket Notification Database available at https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm identifies combination product submissions. The general controls provisions of the Act include requirements for annual registration, listing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration. Please note: CDRH does not evaluate information related to contract liability warranties. We remind you, however, that device labeling must be truthful and not misleading.
If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to additional controls. Existing major regulations affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 898. In addition, FDA may publish further announcements concerning your device in the Federal Register.
Additional information about changes that may require a new premarket notification are provided in the FDA guidance documents entitled "Deciding When to Submit a 510(k) for a Change to an Existing Device" (https://www.fda.gov/media/99812/download) and "Deciding When to Submit a 510(k) for a Software Change to an Existing Device" (https://www.fda.gov/media/99785/download).
1
Your device is also subject to, among other requirements, the Quality System (QS) regulation (21 CFR Part 820), which includes, but is not limited to, 21 CFR 820.30, Design controls; 21 CFR 820.90, Nonconforming product; and 21 CFR 820.100, Corrective and preventive action. Please note that regardless of whether a change requires premarket review. the OS regulation requires device manufacturers to review and approve changes to device design and production (21 CFR 820.30 and 21 CFR 820.70) and document changes and approvals in the device master record (21 CFR 820.181).
Please be advised that FDA's issuance of a substantial equivalence determination does not mean that FDA has made a determination that your device complies with other requirements of the Act or any Federal statutes and regulations administered by other Federal agencies. You must comply with all the Act's requirements, including, but not limited to: registration and listing (21 CFR Part 807); labeling (21 CFR Part 801); medical device reporting of medical device-related adverse events) (21 CFR Part 803) for devices or postmarketing safety reporting (21 CFR Part 4, Subpart B) for combination products (see https://www.fda.gov/combination-products/guidance-regulatory-information/postmarketing-safety-reportingcombination-products); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820) for devices or current good manufacturing practices (21 CFR Part 4, Subpart A) for combination products; and, if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR Parts 1000-1050.
Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to https://www.fda.gov/medical-device-safety/medical-device-reportingmdr-how-report-medical-device-problems.
For comprehensive regulatory information about mediation-emitting products, including information about labeling regulations, please see Device Advice (https://www.fda.gov/medicaldevices/device-advice-comprehensive-regulatory-assistance) and CDRH Learn (https://www.fda.gov/training-and-continuing-education/cdrh-learn). Additionally, you may contact the Division of Industry and Consumer Education (DICE) to ask a question about a specific regulatory topic. See the DICE website (https://www.fda.gov/medical-device-advice-comprehensive-regulatoryassistance/contact-us-division-industry-and-consumer-education-dice) for more information or contact DICE by email (DICE@fda.hhs.gov) or phone (1-800-638-2041 or 301-796-7100).
Sincerely,
Bradley O. Quinn -
Bradley Quinn Assistant Director DHT1C: Division of Sleep Disordered Breathing, Respiratory and Anesthesia Devices OHT1: Office of Ophthalmic, Anesthesia,
2
Respiratory, ENT and Dental Devices Office of Product Evaluation and Quality Center for Devices and Radiological Health
Enclosure
3
Indications for Use
510(k) Number (if known) K230277
Device Name Pulse Oximeter (Model OHT60,OXH78)
Indications for Use (Describe)
The Pulse Oximeter is intended for spot-checking oxygen saturation and pulse rate, and the device is a reusable device and intended to be used with the finger of adults in professional healthcare facility or home conditions when physician follow-up and operated by a physician. And it is not intended to be used under motion.
Type of Use (Select one or both, as applicable)
| ☑ Prescription Use (Part 21 CFR 801 Subpart D) |
|---|
| ☐ Over-The-Counter Use (21 CFR 801 Subpart C) |
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4
510(k) Summary
K230277
This summary of 510(k) safety and effectiveness information is being submitted in accordance with requirements of 21 CFR 807.92.
1.0 Submitter's Information
| Name: | Cofoe Medical Technology Co., Ltd. |
|---|---|
| Address: | No. 87, Section 1 of Huanbao East Road, Yuhua District, |
| 410000 Changsha, Hunan, PEOPLE'S REPUBLIC OF CHINA | |
| Tel: | 86-18674772941 |
| Contact: | Ms. Yang Cui |
| Registration Number: | 3016426850 |
Designated Submission Correspondent
| Contact: | Mr. Boyle Wang |
|---|---|
| Name: | Shanghai Truthful Information Technology Co., Ltd. |
| Address: | Room 1801, No. 161 East Lujiazui Rd., Pudong Shanghai |
| 200120 China | |
| Tel: | +86-21-50313932 |
| Email: | Info@truthful.com.cn |
Date of Preparation: Dec.25,2023
2.0 Device Information
| Trade name: | Pulse Oximeter |
|---|---|
| Common name: | Pulse Oximeter |
| Classification name: | Oximeter |
| Model(s): | Model OHT60, Model OXH78 |
| Production code: | DQA |
| Regulation number: | 21 CFR 870.2700 |
| Classification: | Class II |
| Panel: | Anesthesiology |
3.0 Predicate Device Information
| Manufacturer: | Huizhou Xiaoou Technology Co., Ltd. |
|---|---|
| Trade name: | Pulse Oximeter (Model Number-SO611), Pulse Oximeter (Model |
| Number-SO711), Pulse Oximeter (SO811), Pulse Oximeter |
5
| (SO911) | |
|---|---|
| 510(k) number: | K212665 |
4.0 Indication for Use Statement
The Pulse Oximeter is intended for spot-checking oxygen saturation and pulse rate, and the device is a reusable device and intended to be used with the finger of adults in professional healthcare facility or home conditions when physician follow-up and operated by a physician. And it is not intended to be used under motion.
5.0 Device Description
The pulse oximeter, Model OHT60 and OXH78, consists of probe, electronic circuits, and display and plastic enclosures, is designed for spot checking of the pulse oxygen saturation and pulse rate for adults in a professional healthcare facility or home conditions when physician follow-up and operated by a physician. This medical device can be reused. Not for continuously monitoring.
SpO2 is based on the absorption of pulse blood oxygen to red and infrared light by means of finger sensor and SpO2 measuring unit. The measurement principle of Pulse oximeter is based on the absorption spectrum characteristics of hemoglobin and oxyhemoglobin in red and infrared regions, and the empirical formula of data is established by using ' Lambert Beer ' law. The working principle of the instrument adopts photoelectric blood oxygen detection technology combined with volume pulse recording technology, The specific process is as follows: Firstly, the infrared light emitting at 660 nm and the near-infrared light emitting at 905 are used to irradiate the finger and the measurement data are obtained by the infrared receiver tube. Secondly, the obtained measurement data were calculated and processed by electronic circuits and microprocessors to obtain the blood oxygen saturation and pulse rate, and the calculation results were displayed on the screen.
The subject device is a reusable device, and need to reprocess as suggested in the user manual after each use. And the device is intended to be used on the finger, and powered by 2*1.5V AAA alkaline batteries.
The Model OHT60 and OXH78 have the same critical components and its materials and means of power supply, PCB layout and Software are little different.
6.0 Technological Characteristics
Principle of Operation
The module utilizes the same principles of operation for pulse oximetry governed by the following principles:
- Oxyhemoglobin (oxygenated blood) and deoxyhemoglobin (non-oxygenated blood)
6
differ in their absorption of red and infrared light (spectrophotometry).
The amount of arterial blood in tissue changes with your pulse 2. (photoplethysmography). Therefore, the amount of light absorbed by the varying quantities of arterial blood changes as well.
Mechanism of Action for Achieving the Intended Effect
A mathematic formula is established making use of Lambert Beer Law according to Spectrum Absorption Characteristics of Reductive hemoglobin (RHb) and Oxyhemoqlobin (Hbo2) in red and near-infrared zones. Operation principle of the instrument: Photoeletric Oxyhemoglobin Inspection Technology adopted in accordance with Capacity Pulse Scanning and Recording Technology, so that two beams of different wavelength of lights (660nm red and 905nm near infrared light) can be focused on a human nail tip through a clamping finger-type sensor. A measured signal obtained by a photosensitive element, will be shown on the oximeters display through process in electronic circuits and microprocessor.
7.0 Non-clinical Testing Summary
The following performance data have been conducted to verify that the Oximeter meets all design specifications which supports the conclusion that it's Substantially Equivalent (SE) to the predicate device. The testing results demonstrate that the targeted device complies with the following standards:
Conclusions for Biocompatibility Testing
The biocompatibility evaluation for the oximeter was conducted in accordance with the FDA's Biocompatibility Guidance "Use of International Standard ISO 10993-1, 'Biological Evaluation of Medical Devices - Part 1: Evaluation and Testing Within a Risk Management Process" , as recognized by FDA. The worst case of the whole system is considered tissue contacting for duration of permanent (>30 days). And the testing included the following tests:
Cytotoxicity, per ISO 10993-5, Biological Evaluation Of Medical Devices -- Part 5: Tests For In Vitro Cytotoxicity
Skin Sensitization and Skin Irritation, per ISO 10993-10, Biological Evaluation Of Medical Devices - Part 10: Tests For Irritation And Skin Sensitization
According to the Attachment G: Biocompatibility of Certain Devices in
Contact with Intact Skin of FDA Guidance Use of International Standard ISO10993-1, "Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process", issued on: September 8, 2023. Acrylonitrile butadiene styrene (ABS), Polycarbonate (PC) and Silicone materials are considered to pose a very low biocompatibility risk because they have a long history of safe use in medical devices that contact intact skin.
So the specific biocompatibility testing for Case, Keys and Silicone are not necessary.
7
Electrical and EMC Safety:
The electrical safety and EMC safety testing was performed to, and passed, the following standards:
IEC 60601-1:2005/AMD2:2020, Medical Electrical Equipment - Part 1: General Requirements For Basic Safety And Essential Performance
IEC 60601-1-11 Edition 2.0 2015-01, Medical electrical equipment -- Part 1-11: General requirements for basic safety and essential performance -- Collateral standard: Requirements for medical electrical equipment and medical electrical systems used in the home healthcare environment
IEC 60601-1-2 Edition 4.0 2014-02, Medical electrical equipment -- Part 1-2: General requirements for basic safety and essential performance -- Collateral standard: Electromagnetic disturbances - Requirements and tests
Summary of Bench Testing
Bench testing was conducted and the results show that the subject device complies with the below standard:
ISO 80601-2-61 Second edition 2017-12 (Corrected version 2018-02), Medical electrical equipment - Part 2-61: Particular requirements for basic safety and essential performance of pulse oximeter equipment
Software Verification and Validation Testing
Software documentation including verification & validation was provided in accordance with FDA Guidance: Guidance for the Content of Premarket Submissions for Software Contained in Medical Devices for software with a moderate level of concern.
The Software Validation is in compliance with FDA Guidance.
Summary of Shelf Life and Cleaning Testing
The service life has been verified through accelerated aging. The service life is 5 years except the battery is reasonable and effective.
Cleaning and disinfection validation testing was conducted in accordance with FDA quidance "Reprocessing Medical Devices in Health Care Settings: Validation Methods and Labeling" issued March 17,2015. Moreover, the performance of the subject device shows no degradation after repeated cleaning and disinfection as suggested in the User manual.
8.0 Clinical Test Summary
Clinical studies were conducted at Sir Run Run Shaw Hospital, School of Medicine, Zhejiang University to verify the accuracy of the subject device.
8
The clinical study was conducted in accordance to ISO80601-2-61:2017, ISO14155:2020, and the FDA Guidance Document for Pulse Oximeters. The subject device of this study was to verify the accuracy of pulse oximetry (SpO2) measured by the oximeter with a measurement range of 70-100% in the static state.
The induced Fraction of inspiration O2 (FiO2) control test was performed on subjects, and the subjects were subjected to radial artery puncture and indwelling catheter to obtain a stable arterial blood sample. The pulse oxygen saturation (SpO2) measured by the oximeter is compared with the functional oxygen saturation (SaO2) in arterial blood is analyzed by the arterial blood gas analyzer(CO-OXIMETER).
12 healthy adult volunteer subjects (ages 21-42yr, 46-75kg, 150-180cm, with light to dark pigmentation) were included in the study conducted to evaluate and complete the SpO2 accuracy performance of the Pulse Oximeter. 4 males and 8 females (including 4 subjects with Fitzpatrick V, VI, 8 subjects with Fitzpatrick I ~ Fitzpatrick IV).
| Subject
No | Site | Enrollment
Date | Treatment
Received | Adherence to
Protocol | Adverse
Events |
|---------------|--------------------------------------------------------------------------------|--------------------|-------------------------|--------------------------|-------------------|
| 1~12 | Sir Run Run Shaw
Hospital, 01 School
of Medicine,
Zhejiang University | 2021.07.26 | OHT60 Pulse
Oximeter | Yes | No |
The measure result between the SpO2 measured by subject device and the SaO2 measured by the blood gas analyzer.
The SpO2 accuracy performance results showed the subject Pulse Oximeter to have an ARMS of 1.98 during steady state conditions over the range of 70-100%.
9.0 Technological Characteristic Comparison Table
9
| Item | Subject Device
K230277 | Predicate Device
K2126665 | Remark |
|---------------------------------------|------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|-----------|
| Product Name | Pulse Oximeter | Pulse Oximeter | -- |
| Manufacturer | Cofoe Medical Technology Co., Ltd. | Huizhou Xiaoou Technology Co., Ltd. | -- |
| Product Code | DQA | DQA | Same |
| Regulation No. | 21CFR 870.2700 | 21CFR 870.2700 | Same |
| Class | Class II | Class II | Same |
| Model | OHT60,OXH78 | SO611,SO711,SO811,SO911 | -- |
| Intended
Use/Indication for
Use | The Pulse Oximeter is intended for spot-
checking oxygen saturation and pulse
rate, and the device is a reusable device
and intended to be used with the finger
of adults in professional healthcare
facility or home conditions when
physician follow-up and operated by a
physician. And it is not intended to be
used under motion. | The Pulse Oximeter is intended for spot-
checking oxygen saturation and pulse rate,
and the device is a reusable device
and intended to be used with the finger of
adults in professional healthcare facility or
home conditions when physician
follow-up and operated by a physician. And
it is not intended to be used under motion
or low perfusion scenarios. | Same |
| Principle | The oximeter consists of probe,
electronic circuits, and display and
plastic enclosures. And one side of
probe is designed to locate light emitting
diodes and a light detector (called a
photo-detector). Red and Infrared lights
are shone through the tissues from one
side of the probe to the other. Then
parts of the light emitted absorbed by
blood and tissues. The light absorbed by
the blood varies with the oxygen
saturation of haemoglobin. After that,
the photo-detector detects the light
volume transmitted through the tissues
which depends on blood pulse,
Hereafter, the microprocessor calculates
a value for the oxygen saturation
(SpO2). | The oximeter consists of probe, electronic
circuits, and display and plastic enclosures.
And one side of probe is designed to locate
light emitting diodes and a light detector
(called a photo-detector). Red and Infrared
lights are shone through the tissues from
one side of the probe to the other. Then
parts of the light emitted absorbed by blood
and tissues. The light absorbed by the
blood varies with the oxygen saturation of
haemoglobin. After that, the photo-detector
detects the light volume transmitted
through the tissues which depends on
blood pulse, Hereafter, the microprocessor
calculates a value for the oxygen
saturation (SpO2). | Same |
| Applied
Population | Adults in home & hospital | Adults in home & hospital | Same |
| Application sites | Finger | Finger | Same |
| Display Type | LED | LED | Same |
| Display Content | OHT60: Display the SPO2, PR, pulse
intensity histogram, Oxygen saturation
value of pulse and battery power status.
OXH78: Display the SPO2, PR, pulse
intensity histogram, perfusion
index, pulse waveforms and battery power
status | Display the SpO2%, PR, battery indicator,
Pulse rate bar graph, pulse waveform | Similar |
| Contacting
material | Shell: ABS
Clip pad: Silicon
Key:PC | Not Publicly available | Different |
| Item | Subject Device
K230277 | Predicate Device
K212665 | Remark |
| Model | OHT60, OXH78 | SO611,SO711,SO811,SO911 | / |
| LED wavelength | Red= 660 nm; Infrared=905nm | Red= 660 nm; Infrared=905nm | Same |
| Power source | 21.5V AAA alkaline battery | 21.5V AAA alkaline battery | Same |
| Display | OHT60: SpO2%; PR; battery level; Pulse
intensity histogram.
OXH78: SpO2%; PR; battery level; Pulse
intensity histogram, Pulse wave form | SpO2%; PR | Same |
| SpO2 Measuring
Range | 35%-100% | 0%-100% | Different |
| SpO2 Resolution | 1% | 1% | Same |
| SpO2 Accuracy | 70100%, ±3%;100%, ±2%;
0% to 69%: unspecified | 70
0% to 69%: unspecified | Similar |
| PR Measuring
Range | 30-250BPM | 30-250BPM | Same |
| PR Resolution | 1 bpm | 1 bpm | Same |
| PR Accuracy | ± 3bpm | ± 3bpm | Same |
Table1-General Comparison
Analysis:
Materials of the predicate device is not publicly available. The
biocompatibility evaluation has performed and passed on the subject device and the predicate device per the International Standard ISO 10993-1 "Biological Evaluation of Medical Devices - Part 1: Evaluation and Testing Within a Risk Management Process," as recognized by FDA.
10
Table 2 Performance Comparison
Analysis:
The SpO2 measurement range and accuracy is a little different, but they are within the limits of the specified range of the standard ISO 80601-2-61 and FDA guidance for Pulse Oximeters. The different has no effect on substantive equivalence.
Table 3 Safety Comparison
| Item | Subject Device
K230277 | Predicate Device
K212665 | Remark |
|-------------------|-------------------------------------------|-------------------------------------------|--------|
| Electrical Safety | Comply with IEC 60601-1
IEC 60601-1-11 | Comply with IEC 60601-1
IEC 60601-1-11 | Same |
| EMC | Comply with IEC 60601-1-2 | Comply with IEC 60601-1-2 | Same |
| Performance | ISO 80601-2-61 | ISO 80601-2-61 | Same |
| Biocompatibility | Comply with ISO 10993-1,
FDA Guidance | Comply with ISO 10993-1,
FDA Guidance | Same |
10.0 Conclusion
The conclusions drawn from the comparison and analysis above demonstrate that the subject device is substantially equivalent to the legally marketed predicated device.