Corpak Co.
Corpak Co. holds FDA 510(k) medical device clearances, first cleared 1981, most recent 1996.
Top product codes for Corpak Co.
Recent clearances by Corpak Co.
- K935512 — CORPAK REPLACEMENT GASTROSTOMY DEVICE STOMACORE
- K931921 — CORPAK GASTROSTOMY TUBE
- K932847 — CORPAK ENTERAL PUMP
- K902949 — CORPAK GRASPING FORCEPS
- K901501 — CORPAK GASTROSTOMY TUBE
- K882867 — CORPAK PERCUTANEOUS ENDOSCOPIC GASTROSTOMY TUBE
- K853253 — CORPAK FARRELL VALVE ENTERAL GASTRIC PRESSURE RELI
- K852792 — CORPAK ENTERAL SOL ADM PUMP SET W/ SCREW
- K842257 — CORPAK URINARY DRAINAGE BAG
- K841819 — CORPAK FOLEY CATH TRAY W/16FR. TEFLON
- K840292 — URETHRAL CATH. TRAY W/BAG
- K832167 — CORPAK VTR 300 ENTERNAL PUMP
- K830965 — ENTERAL SOLUTION ADMIN. PUMP SET
- K821409 — CORPAK-ENTERAL FEEDING CONTAINER
- K821410 — CORPAK-MONITOR ENTERAL FEEDING CONTAIN
- K820952 — OPTI-MIST
- K821036 — ENTERNAL SOLUTION ADMIN. SET
- K810559 — OPTI- SYSTEM
- K810217 — NEBULIZER HEATER
- K810218 — PREFILLED NEBULIZER
- K810219 — PREFILLED HUMIDIFER
Data sourced from openFDA. This site is unofficial and independent of the FDA.