# Gerard Medical Enterprises, Inc.

- Location (FDA's records): Charlton, MA
- FDA decisions: 8 (1981–1996): 8 510(k) clearances
- Product codes: LJT (5), FMF (2), KRC (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 13 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Gerard Medical, Inc.: 1 (https://510kreport.com/company/gerard-medical)

## Its most-cited devices
- K942623: Trimport (1994), cited by 1

## Recent decisions
- K954258: Trimport Implantable Access System (Modification) (May 24, 1996)
- K945250: Trimport (Mar 7, 1995)
- K942623: Trimport (Aug 23, 1994)
- K922147: Dual Plastic Vascular Access System (Dec 4, 1992)
- K913114: Trim-Port (TM) Implant Access Syst Dual Titan Port (Jan 2, 1992)
- K912111: Modified Version Implantable Vascular Access Syste (Oct 8, 1991)
- K903364: Gerard Medical, Inc. Trim-Port (Oct 31, 1990)
- K813358: Gerard Medical Electrode Tester (Dec 29, 1981)

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