# K952491: MODEL 7355

- Pathway: 510(k) (Traditional)
- Applicant: Devilbiss Health Care, Inc.
- Decided: Jan 31, 1996 after 246 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
No predicates in its family tree.
5 later devices descend from it; 1 cites it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K032056: Bilevel Cpap, Model 9055 Series (2004), 4 descendants of its own
- K091919: Devilbiss Intellipap/Sleepcube Bilevel S/ST (2009), 1 descendant of its own
- K112220: Devilbiss Intellipap / Sleepcube Auto Bilevel (2011), 0 descendants of its own
- K093070: Devilbiss Intellipap/ Sleepcube Bilevel ST, DV56 ST Series (2010), 0 descendants of its own
- K043282: Devilbiss Autoadjust, Model 9054 Series (2005), 0 descendants of its own

Source page: https://510kreport.com/device/K952491
Methodology: https://510kreport.com/methodology