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

CORPAK FOLEY CATH TRAY W/16FR. TEFLON

K Number: K841819 · Decision Jul 19, 1984
Classifications
1
FEI Numbers
114
Registration Numbers
114
Same Product Code
237
Applicant Total
21
Review Days
78

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Basic Information

Device Name
CORPAK FOLEY CATH TRAY W/16FR. TEFLON
K Number
K841819
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5130
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Corpak Co.
Date Received
May 2, 1984
Decision Date
July 19, 1984
Product Code
KOD
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
KOD Catheter, Urological

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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
K840292 URETHRAL CATH. TRAY W/BAG
Search all 21 clearances from Corpak Co. →