# Medcor, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 8 (1977–1980): 8 510(k) clearances
- Product codes: DXY (6)
- Predicates its devices cite: 0 (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

## Recent decisions
- K792609: Lithicron 0520 P-Synchroneous Pulse Gen. (Nov 19, 1980)
- K802224: Quintrex 0516 Prog. Pulse Generator Sys (Sep 12, 1980)
- K802223: Quintrex 0515 Programmable Pulse Gen. (Sep 12, 1980)
- K791678: Lithicron II 0403 Implantable Pacemaker (Sep 7, 1979)
- K791095: Lithicron Model 0401, Pacemaker (Aug 10, 1979)
- K780430: Lithicron F Programmable Pulse Gen (Dec 22, 1978)
- K771538: Lithicron Model 3-70C-B Pulse Generator (Aug 22, 1977)
- K770507: Pulse Generator, Litkicron Model 3-70H (Apr 7, 1977)

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