# K092264: Atlantis Hyperbaric Chamber Ventilator

- Pathway: 510(k) (Traditional)
- Applicant: Providence Global Medical, Inc.
- Decided: Dec 17, 2009 after 142 days
- Product code: CBK (Ventilator, Continuous, Facility Use)
- Device class: 2
- Regulation: 21 CFR 868.5895
- 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 K082351 (2009). 1 ancestor in all.
1 later device descends from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K082351: Neptune Hyperbaric Ventilator, Level-5, Inc. (2009) Summary page 4.

## Most influential descendants
- K122560: Versalvent Model V1 Hyperbaric Chamber Ventilator Model V1 (2013), 0 descendants of its own

## Indications for use
The Atlantis Hyperbaric Ventilator is indicated for use with pediatric and adult patients in respiratory failure or any other specific patient breathing requirements, as determined by the attending physician, when the patient is placed inside a hyperbaric chamber for prescribed therapy.

Source page: https://510kreport.com/device/K092264
Methodology: https://510kreport.com/methodology