# Pryon Corp.

- Location (FDA's records): Menomonee Falls, WI
- FDA decisions: 4 (1992–1994): 4 510(k) clearances
- Product codes: CCK (3), DQA (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 2 (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
- Mennen Medical, Inc.: 1 (https://510kreport.com/company/mennen-medical)
- Natus Medical, Inc.: 1 (https://510kreport.com/company/natus-medical)

## Its most-cited devices
- K935272: CAP 400 AT (1994), cited by 2

## Recent decisions
- K942772: A-200 Multi-Use Airway Adapter (Jul 25, 1994)
- K935272: CAP 400 AT (Jul 13, 1994)
- K930250: Low Dead Space Adaptor & Reuasable Airway Adaptor (Oct 15, 1993)
- K915773: P-300 Capnograph and Pulse Oximeter (Jun 24, 1992)

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