# Pulmonox Medical, Inc.

- Location (FDA's records): Edmonton, Ab, CA
- FDA decisions: 3 (2000–2004): 3 510(k) clearances
- Names in FDA's records: Pulmonox Medical, Inc. (2); Pulmonox Medical Corp. (1)
- Product codes: MRN (2), MRP (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 3 (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 that cite its devices most
- Ino Therapeutics: 2 (https://510kreport.com/company/ino-therapeutics)
- International Biomedical: 1 (https://510kreport.com/company/international-biomedical)

## Its most-cited devices
- K000653: Aeronox Universal, Model P/N 360000, Aeronox Bedside, Model P/N 360001, Aeronox Transport Transport, Model P/N 360002 (2000), cited by 2
- K023014: Vianox Delivery System, Model I (2003), cited by 1

## Recent decisions
- K033779: Vianox Delivery System, Model II (Jan 26, 2004)
- K023014: Vianox Delivery System, Model I (Aug 14, 2003)
- K000653: Aeronox Universal, Model P/N 360000, Aeronox Bedside, Model P/N 360001, Aeronox Transport Transport, Model P/N 360002 (Aug 4, 2000)

Source page: https://510kreport.com/company/pulmonox-medical