# Gil-Med Industries C/O Kegan & Kegan, Ltd.

- Location (FDA's records): Chicago, IL
- FDA decisions: 7 (1984–1988): 7 510(k) clearances
- Product codes: KPE (4), KNT (2), KNX (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: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K880506: Modified Eva-Mix and DI-Mix Bags (May 20, 1988)
- K870274: DI-Mix Parenteral Nutrition & Medicine Container (Feb 10, 1987)
- K861862: Dieto Container for Enteral Nutrition (Aug 11, 1986)
- K841597: Gil-Med Parenteral Nutrition or Medicine (Oct 26, 1984)
- K841224: Uro-Male Incontinence Catheter (May 2, 1984)
- K840915: Dimix Container for Parneteral Nutrit (Apr 17, 1984)
- K840916: Dieto Container for Enternal Nutrit (Apr 4, 1984)

Source page: https://510kreport.com/company/gil-med-industries-c-o-kegan-kegan