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

URETHRAL CATH. TRAY W/BAG

K Number: K840292 · Decision Mar 16, 1984
Classifications
1
FEI Numbers
127
Registration Numbers
127
Same Product Code
205
Applicant Total
21
Review Days
52

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Basic Information

Device Name
URETHRAL CATH. TRAY W/BAG
K Number
K840292
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5250
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Corpak Co.
Date Received
January 24, 1984
Decision Date
March 16, 1984
Product Code
KNX
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
KNX Collector, Urine, (And Accessories) For Indwelling Catheter

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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
K852792 CORPAK ENTERAL SOL ADM PUMP SET W/ SCREW
K842257 CORPAK URINARY DRAINAGE BAG
K841819 CORPAK FOLEY CATH TRAY W/16FR. TEFLON
Search all 21 clearances from Corpak Co. →