FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

CORPAK GRASPING FORCEPS

K Number: K902949 · Decision Aug 30, 1990
Classifications
1
FEI Numbers
50
Registration Numbers
50
Same Product Code
73
Applicant Total
21
Review Days
56

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Basic Information

Device Name
CORPAK GRASPING FORCEPS
K Number
K902949
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Corpak Co.
Date Received
July 5, 1990
Decision Date
August 30, 1990
Product Code
OCZ
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

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

Product Code Device Name
OCZ Endoscopic Grasping/Cutting Instrument, Non-Powered

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Other Clearances by Corpak Co.

K Number Device Name
K935512 CORPAK REPLACEMENT GASTROSTOMY DEVICE STOMACORE
K931921 CORPAK GASTROSTOMY TUBE
K932847 CORPAK ENTERAL PUMP
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. →