# Phoenix Biomedical Corp.

- Location (FDA's records): Valley Forge, PA
- FDA decisions: 13 (1996–2004): 13 510(k) clearances
- Names in FDA's records: Phoenix Biomedical Corp. (12); Phoenix Biomedical (1)
- Product codes: JXG (11), GAS (1), MKY (1)
- Predicates its devices cite: 3 (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
- Dicomit Imaging Systems Corp.: 1 (https://510kreport.com/company/dicomit-imaging-systems)
- Advanced Technology Laboratories, Inc.: 1 (https://510kreport.com/company/advanced-technology-laboratories)
- GE Medical Systems: 1 (https://510kreport.com/company/ge-medical-systems)

## Recent decisions
- K033017: Phoenix Infusion Catheter (Apr 7, 2004)
- K030468: Acura Elite Gravity Compensating Reservoir (Oct 15, 2003)
- K024101: Phoenix Universal Shunt System (Jan 27, 2003)
- K024040: Accura Elite Shunt System (Jan 27, 2003)
- K021644: Perf (Ommaya Style) Reservoirs (Aug 6, 2002)
- K002476: Lumboperitoneal Shunt System (Nov 9, 2000)
- K000514: Rumbar Drainage System (May 10, 2000)
- K991429: Diamond II Valve (May 19, 1999)

Source page: https://510kreport.com/company/phoenix-biomedical