# Cormed, Inc., Sub. C.R.Bard, Inc.

- Location (FDA's records): Medina, NY
- FDA decisions: 8 (1983–1986): 8 510(k) clearances
- Product codes: LJS (2), LJT (2), FRN (1), GAA (1), FMI (1), DYB (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 2 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Plastimed Laboratoire Pharmaceutique: 1 (https://510kreport.com/company/plastimed-laboratoire-pharmaceutique)
- Specialized Health Products, Inc.: 1 (https://510kreport.com/company/specialized-health-products)

## Its most-cited devices
- K823553: Corcath H & B Vascular Access Catheter (1983), cited by 1
- K863606: Butterfly Non-Coring Needle Set (1986), cited by 1

## Recent decisions
- K863606: Butterfly Non-Coring Needle Set (Dec 18, 1986)
- K860432: Percutaneous Introducer Kit (Mar 31, 1986)
- K854019: Port-Gard (Nov 26, 1985)
- K850967: Sterile Cormed Mediport (May 17, 1985)
- K850674: Cormed II Ambulatory Infusion Pump (Apr 9, 1985)
- K843083: Cormed Huber Point Needle (Sep 5, 1984)
- K833915: Vascular Access Cath. Repair Kit (Mar 30, 1984)
- K823553: Corcath H & B Vascular Access Catheter (Jan 5, 1983)

Source page: https://510kreport.com/company/cormed-sub-crbard
