# General Medical Co.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 15 (1977–1993): 15 510(k) clearances
- Product codes: EGJ (2), FRG (2), KMJ (2), EFQ (1), FSM (1), BSY (1), FYC (1), FHX (1), BTM (1), FME (1), LRO (1), KXF (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 3 (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
- Hidrex GmbH: 1 (https://510kreport.com/company/hidrex)
- Carefusion 2200, Inc.: 1 (https://510kreport.com/company/carefusion-2200)
- Allegiance Healthcare Corp.: 1 (https://510kreport.com/company/allegiance-healthcare)

## Its most-cited devices
- K844652: C.a.S.E. Container (1984), cited by 2
- K831320: Drionic (1983), cited by 1

## Recent decisions
- K926269: Procedure Kit (Aug 27, 1993)
- K912975: Operand Lubricating Jelly (Sep 27, 1991)
- K912132: Operand Lubricating Jelly (Aug 7, 1991)
- K903669: Genesis Insufflating Catheter (Sep 12, 1990)
- K900110: Operand* Lubricating Jelly (May 2, 1990)
- K853635: Subderm  TM (Dec 20, 1985)
- K844652: C.a.S.E. Container (Dec 12, 1984)
- K831320: Drionic (Jul 19, 1983)

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