# Oscor Medical Corp.

- Location (FDA's records): Palm Harbor, FL
- FDA decisions: 31 (1985–1997): 31 510(k) clearances
- Product codes: DTB (22), LDF (4), DYB (1), LQR (1), DTE (1), DTD (1), DTC (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 5 (0 its own)
- Recalls linked to its devices: 2 (1 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Osypka Medical, Inc.: 3 (https://510kreport.com/company/osypka-medical)
- Medtronic Vascular: 1 (https://510kreport.com/company/medtronic-vascular)
- Osypka AG: 1 (https://510kreport.com/company/osypka)

## Its most-cited devices
- K923621: External Demand Pacemaker (1993), cited by 3
- K850622: Oscor Medical Model Tme 64S Bipolar Temp/Heart Wir (1985), cited by 2

## Recent decisions
- K964107: Oscor Permanent Retractable Screw-in Pacing Lead Model PR (Apr 1, 1997)
- K925168: Miscellaneous Pacing Lead (May 3, 1994)
- K923621: External Demand Pacemaker (May 19, 1993)
- K912867: Oscor Medical Corp Permanent Pacing Lead (Feb 4, 1992)
- K915008: Permanent Pacing Pad, Modification (Jan 27, 1992)
- K915007: Permanent Pacing Leads, Modification (Jan 27, 1992)
- K913204: Model KY Pacemaker Lead-Various, Modification (Sep 23, 1991)
- K913202: Implant Pacing Lead, Tined #3262, Modification (Sep 23, 1991)

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