# Med General

- Location (FDA's records): Mchenry, IL
- FDA decisions: 12 (1977–1979): 12 510(k) clearances
- Product codes: GDJ (2), GXY (2), BXN (1), IPF (1), DXC (1), KDC (1), GZJ (1), GCY (1), DRT (1), ISB (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K791097: Ceptortrode with Ceptor Hesive (Aug 3, 1979)
- K791098: Single-Use Mini-Bulldog (Jun 22, 1979)
- K790763: Maxi-Vac TM (Apr 23, 1979)
- K790269: Ceptor Hesive (Feb 26, 1979)
- K782006: Medgeneral Single-Use Bulldog (Dec 15, 1978)
- K781239: Myo-Stim (Nov 3, 1978)
- K780632: Maxiceptor (Aug 14, 1978)
- K780698: Stimulators, Nerve, Electrical (May 12, 1978)

Source page: https://510kreport.com/company/med-general