FDA 510(k) FDA class 2 Substantially Equivalent - Subject to Tracking Reg. 🇺🇸 United States

CORPAK ENTERAL PUMP

K Number: K932847 · Decision Jun 17, 1994
Classifications
1
FEI Numbers
149
Registration Numbers
149
Same Product Code
847
Applicant Total
21
Review Days
372

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Basic Information

Device Name
CORPAK ENTERAL PUMP
K Number
K932847
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5725
Medical Specialty
General Hospital
Decision
Substantially Equivalent - Subject to Tracking Reg.
Applicant
Corpak Co.
Date Received
June 10, 1993
Decision Date
June 17, 1994
Product Code
FRN
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
FRN Pump, Infusion

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Other Clearances by Corpak Co.

K Number Device Name
K935512 CORPAK REPLACEMENT GASTROSTOMY DEVICE STOMACORE
K931921 CORPAK GASTROSTOMY TUBE
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
Search all 21 clearances from Corpak Co. →