# K102625: Vega Cpap System/Heated Humidifier, Model CP-03

- Pathway: 510(k) (Traditional)
- Applicant: Vega Technologies, Inc.
- Decided: Jun 10, 2011 after 270 days
- Product code: BZD (Ventilator, Non-Continuous (Respirator))
- Device class: 2
- Regulation: 21 CFR 868.5905
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K010263 (2001). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K010263: Remstar Plus Cpap System, Respironics, Inc. (2001) Summary page 1.

## Indications for 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.

Source page: https://510kreport.com/device/K102625
Methodology: https://510kreport.com/methodology