# Corpak Co.

- Location (FDA's records): Wheeling, IL
- FDA decisions: 24 (1981–1998): 24 510(k) clearances
- Names in FDA's records: Corpak Co. (21); Corpak, Inc. (3)
- Product codes: KNT (10), CAF (3), FRN (3), BTT (2), KNX (2), KGC (1), KOD (1), OCZ (1), FKO (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: 15 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Boston Scientific Corp: 1 (https://510kreport.com/company/boston-scientific)
- Alexander Mfg. Co.: 1 (https://510kreport.com/company/alexander-mfg)

## Its most-cited devices
- K832167: Corpak VTR 300 Enternal Pump (1983), cited by 1
- K901501: Corpak Gastrostomy Tube (1990), cited by 1

## Recent decisions
- K964514: Corpak Medsystems Cruz Catheter for Peritoneal Dialysis (Jun 26, 1998)
- K970178: Clog Zapper Enteral Feeding Tube Declogging System (Jul 21, 1997)
- K935512: Corpak Replacement Gastrostomy Device Stomacore (Aug 29, 1996)
- K944750: Corflo 300 Pump (Jun 19, 1995)
- K931921: Corpak Gastrostomy Tube (Jun 9, 1995)
- K932847: Corpak Enteral Pump (Jun 17, 1994)
- K902949: Corpak Grasping Forceps (Aug 30, 1990)
- K901501: Corpak Gastrostomy Tube (Jun 11, 1990)

Source page: https://510kreport.com/company/corpak