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

KENGUARD URINARY DRAINAGE BAG W/ANTIREFLUX CHAMBER

K Number: K931459 · Decision Jun 14, 1993
Classifications
1
FEI Numbers
127
Registration Numbers
127
Same Product Code
205
Applicant Total
66
Review Days
83

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Basic Information

Device Name
KENGUARD URINARY DRAINAGE BAG W/ANTIREFLUX CHAMBER
K Number
K931459
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5250
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Kendall Healthcare Products Co. Div.Of Tyco Health
Date Received
March 23, 1993
Decision Date
June 14, 1993
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 Kendall Healthcare Products Co. Div.Of Tyco Health

K Number Device Name
K973763 KENDALL CURITY IODOFORM PACKING STRIP
K973511 KENDALL CURITY PETROLATUM GAUZE
K973507 KENDALL XEROFORM PETROLATUM DRESSING (6311,6312,6313,6314,6315,6316,6317)
K973619 KENDALL CURITY NON-ADHERING DRESSING
K973509 KENDALL CURASORB ZN + MG ALGINATE WOUND DRESSING
K973546 KENDALL FAST-CATH PRE LUBRICATED URETHRAL CATHETER
K970266 KENDALL HYDROPHILIC POWDER WOUND DRESSING
K963446 KENDALL DUAL LUMEN CATHETER
K964899 KENDALL CURITY URETERAL CATHETER
K964519 CURITY THORACENTESIS TRAY
Search all 66 clearances from Kendall Healthcare Products Co. Div.Of Tyco Health →