# Pneumrx, Inc.

- Location (FDA's records): Mountain View, CA
- FDA decisions: 1 (2005–2005): 1 510(k) clearance
- Product codes: KNW (1)
- Predicates its devices cite: 29 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Medical Device Technologies, Inc.: 6 (https://510kreport.com/company/medical-device-technologies)
- Inrad: 3 (https://510kreport.com/company/inrad)
- Promex, Inc.: 3 (https://510kreport.com/company/promex)
- Urological, Inc.: 1 (https://510kreport.com/company/urological)
- Biopsy Sciences, LLC: 1 (https://510kreport.com/company/biopsy-sciences)
- Boston Scientific Corp: 1 (https://510kreport.com/company/boston-scientific)
- Ispg, Inc.: 1 (https://510kreport.com/company/ispg)
- Ethicon Endo-Surgery, Inc.: 1 (https://510kreport.com/company/ethicon-endo-surgery)

## Recent decisions
- K052435: Pneumrx Family of Biopsy Needles and Kits (Nov 3, 2005)

Source page: https://510kreport.com/company/pneumrx