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

CORPAK ENTERAL SOL ADM PUMP SET W/ SCREW

K Number: K852792 · Decision Aug 8, 1985
Classifications
1
FEI Numbers
242
Registration Numbers
243
Same Product Code
648
Applicant Total
21
Review Days
38

Basic Information

Device Name
CORPAK ENTERAL SOL ADM PUMP SET W/ SCREW
K Number
K852792
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5980
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
CORPAK CO.
Date Received
July 1, 1985
Decision Date
August 8, 1985
Product Code
KNT
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
KNT Tubes, Gastrointestinal (And Accessories)

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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
K902949 CORPAK GRASPING FORCEPS
K901501 CORPAK GASTROSTOMY TUBE
K882867 CORPAK PERCUTANEOUS ENDOSCOPIC GASTROSTOMY TUBE
K853253 CORPAK FARRELL VALVE ENTERAL GASTRIC PRESSURE RELI
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. →