# K020932: Devilbiss Pulmo-Aide Compact Compressor

- Pathway: 510(k) (Traditional)
- Applicant: Sunrise Medical
- Decided: Jun 28, 2002 after 98 days
- Product code: CAF (Nebulizer (Direct Patient Interface))
- Device class: 2
- Regulation: 21 CFR 868.5630
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K922623 (1992). 3 ancestors in all.
3 later devices descend from it; 3 cite it directly.
0 of 7 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K970289: Compressor/Nebulizer #3650, Devilbiss Health Care, Inc. (1997) Summary page 1.

## Most influential descendants
- K161586: The JLN-23XX Series Piston Compress Nebulizer (with models JLN-2300AS, JLN-2301AS, JLN-2317AS and JLN-2320AS) (2017), 0 descendants of its own
- K082878: Nevoni Classic, Model 6600-PO (2008), 0 descendants of its own
- K062952: C300 Series Air Nebulizer Compressor (2007), 0 descendants of its own

## Indications for use
The DeVilbiss compressor / nebulizer Model 3655 includes an AC powered air compressor that provides a source of compressed air for home health care use. The compressor is used in conjunction with a jet (pneumatic) nebulizer to convert certain inhalable drugs into an aerosol form for inhalation by a patient. The device can be used with adult or pediatric patients.

Source page: https://510kreport.com/device/K020932
Methodology: https://510kreport.com/methodology