The VEGA CPAP System/Heated Humidifier, models CP-03 delivers positive airway pressure therapy for the treatment of Obstructive Sleep Apnea only. The device is intended for use in the home or hospital/institutional environment on adult patients.

Device Description

The VEGA CPAP System/Heated Humidifier, models CP-03 is a smaller and lighter AC -powered, micro processor-controlled, and blower-based system that generates positive airway pressure from 3 to 20 cm H2O. The device is intended for use with a patient circuit that is used to connect the device to the patient interface(mask). The CPAP device may also be used with VEGA Heated Humidifier that has been designed to be compatible with the CPAP and controlled from the CPAP. The basic functional and performance characteristics of the VEGA CPAP System/Heated Humidifier are completely similar to the predicate device, the Respironics REMstar Plus CPAP System/REMstar Heated Humidifier(K010263).

AI/ML Overview

The provided text does not contain information about acceptance criteria or a study proving that a device meets such criteria in the context of a medical device's performance characteristics or clinical outcomes. Instead, it describes a 510(k) summary for a CPAP system and heated humidifier, focusing on its substantial equivalence to a predicate device, technical specifications, and non-clinical verification activities.

Specifically:

The document mentions "Performance Compliance Test for CPAP according to ISO 17510-1" and "Performance Compliance Test for heated humidifier according to ISO 17510-1" as non-clinical tests conducted by the manufacturer. However, it does not specify what the acceptance criteria for these tests were (e.g., specific pressure accuracy ranges, flow rate tolerances, temperature stability) nor does it report the device's performance against any such criteria.
It explicitly states: "No any Clinical Test is conducted for the VEGA CPAP System/Heated Humidifier." This means there is no clinical study to demonstrate effectiveness or patient outcomes, which would typically be associated with acceptance criteria for device performance in a clinical setting.
The document primarily relies on "substantial equivalence" to a predicate device (Respironics REMstar Plus CPAP System/REMstar Heated Humidifier, K010263) based on similar intended use and technological characteristics, and verification/validation tests for electrical safety and EMC.

Therefore, I cannot provide the requested table or answer most of the questions because the necessary information (acceptance criteria, reported performance against those criteria, details of a performance study, sample sizes, ground truth, expert qualifications, etc.) is not present in the provided 510(k) summary.

In summary, the document does not describe a study that proves the device meets specific acceptance criteria in the way a clinical trial or a detailed performance validation report would.

Summary

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510(K) SUMMARY

JUN 1 0 2011

This summary of 510(k) safety and effectiveness information is being prepared in accordance with the requirements of SMDA 1990 and 21 CFR 807.92 at June 10, 2010.

The assigned 510(k) number is: K1026 25

Submitter's Identifications: Establishment: DONGGUAN DALANG VIGOR ELECTRONICS MFY. Yang Wu District, Da Lang Town, Dong Guan City Guang Dong Prov., CHINA Registration Number: 9616843 Operations: Manufacturer Status: Active Date Of Registration Status: 2004

Owner/Operator: VEGA TECHNOLOGIES, INC. 11F-13, 100 Chang-Chun Rd., Taipei CHINA (Taiwan) 104. Owner/Operator Number: 9036509

Contact: Mr. Joseph Lu VEGA TECHNOLOGIES, INC. I1F-13, 100 Chang-Chun Rd. Taipei, CHiNA (TAIWAN) 104 Phone: 886-2-2541-6996 Fax: 886-2-2521-3803

1. Name of the Device: VEGA CPAP System/Heated Humidifier, model CP-03.
1. Information of the 510(k) Cleared Device (Predicate Device): Respironics REMstar Plus CPAP System/REMstar Heated Humidifier(K010263).

4. Device Description:

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1. Intended Use:
  The VEGA CPAP System/Heated Humidifier, models CP-03 delivers positive airway pressure therapy for the treatment of Obstructive Sleep Apnea only. The device is intended for use in the home or hospital/institutional environment on adult patients.

6. Comparison to the 510(k) Cleared Device (Predicate Device):

The VEGA CPAP System/Heated Humidifier, models CP-03 is substantially equivalent to the Respironics REMstar Plus CPAP System/REMstar Heated Humidifier(K010263). The main technological modification made to CP-03 as it relates to the predicate device includes the followina four issues:

1> the characteristics of delivering air flow(including pressure range, and the related flow rate)
2> the operation and storage environment range.
the device outlook, dimensions, and weight. 3>
4> the main power rating of air compressing motor/heating unit, control IC, and circuit, as well as software.
1. Discussion of Non-Clinical Tests Verification Activities Performed to Determine the Safety and Performance of CP-03 are as the followings:
- 1> Performance Compliance Test for CPAP according to ISO 17510-1 conducted by manufacturer.
- 2> Performance Compliance Test for heated humidifier according to ISO 17510-1 conducted bv manufacturer.
- 3> Electrical Safety Compliance Test according to IEC 60601-1 by accredited laboratory.
- 4> EMC Compliance Test according to IEC 60601-1-2 by accredited laboratory.
1. Discussion of Clinical Test Validation Activities Performed to Determine the Effectiveness of Device are as the followings:

No any Clinical Test is conducted for the VEGA CPAP System/Heated Humidifier.

1. Conclusions
  The VEGA CPAP System/Heated Humidifier, models CP-03, has the same intended use and technological characteristics as the cleared device of Respironics REMstar Plus CPAP System/REMstar Heated Humidifier(K010263). Moreover, verification and validation tests contained in this submission demonstrate that the difference in the submitted demonstrate that the difference in the submitted models could maintain the same safety and effectiveness as that of cleared device.

In the other words, those engineering difference do not: (1) affect the intended use or (2) alter the fundamental scientific technology of the device.

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Image /page/2/Picture/1 description: The image shows the logo for the Department of Health & Human Services-USA. The logo is circular in shape, with the text "DEPARTMENT OF HEALTH & HUMAN SERVICES-USA" arranged around the perimeter of the circle. Inside the circle is an abstract symbol that resembles an eagle or bird in flight. The symbol is composed of three curved lines that suggest the wings and body of the bird.

Food and Drug Administration 10903 New Hampshire Avenue Document Control Room -WO66-G609 Silver Spring, MD 20993-0002

Mr. Joseph Lu Official Correspondent VEGA Technologies, Incorporated 11F-13, 100 Chang-Chun Road Taipei CHINA (TAIWAN) 104

JUN 1 0 2011

Re: K102625

Trade/Device Name: VEGA CPAP System/Heated Humidifier, Models CP-03 Regulation Number: 21 CFR 868.5905 Regulation Name: Noncontinuous Ventilator (IPPB) Regulatory Class: II Product Code: BZD, BTT Dated: May 13, 2011 Received: May 19, 2011

Dear Mr. Lu:

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 (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. 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.

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Page 2 - Mr. Lu

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 (reporting of medical device-related adverse events) (21 CFR 803); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820); and if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050.

If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please go to

http://www.fda.gov/AboutFDA/CentersOffices/CDRH/CDRHOffices/ucm115809.htm for the Center for Devices and Radiological Health's (CDRH's) Office of Compliance. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to

http://www.fda.gov/MedicalDevices/Safety/ReportaProblem/default.htm for the CDRH's Office of Surveillance and Biometrics/Division of Postmarket Surveillance.

You may obtain other general information on your responsibilities under the Act from the Division of Small Manufacturers, International and Consumer Assistance at its toll-free number (800) 638-2041 or (301) 796-7100 or at its Internet address http://www.fda.gov/MedicalDevices/ResourcesforYou/Industry/default.htm.

Sincerely vours.

Wh for

Anthony D. Watson, B.S., M.S., M.B.A. Director Division of Anesthesiology, General Hospital, Infection Control and Dental Devices Office of Device Evaluation Center for Devices and Radiological Health

Enclosure

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Indications For Use

510(k) Number (if known):_

Device Name: VEGA CPAP System/Heated Humidifier, models CP-03.

Indications For Use:

Prescription Use (Part 21 CFR 801 Subpart D) OR

Over-The-Counter Use (21 CFR 807 Subpart C)

(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED)

Concurrence of CDRH, Office of Device Evaluation (ODE)

L. Schulten

(Division Sign-Off) Division of Anesthesiology, General Hospital Infection Control, Dental Devices

Page 1 of

510(k) Number: K102625

Regulation Number and Section

§ 868.5905 Noncontinuous ventilator (IPPB).

(a)
Identification. A noncontinuous ventilator (intermittent positive pressure breathing-IPPB) is a device intended to deliver intermittently an aerosol to a patient's lungs or to assist a patient's breathing.(b)
Classification. Class II (performance standards).