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

URINARY DRAINAGE BAG, (REORDER NO. 0749 - PRODUCT NO. 900-749)

K Number: K962652 · Decision Oct 4, 1996
Classifications
1
FEI Numbers
127
Registration Numbers
127
Same Product Code
205
Applicant Total
36
Review Days
88

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Basic Information

Device Name
URINARY DRAINAGE BAG, (REORDER NO. 0749 - PRODUCT NO. 900-749)
K Number
K962652
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5250
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Customed, Inc.
Date Received
July 8, 1996
Decision Date
October 4, 1996
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 Customed, Inc.

K Number Device Name
K974647 FANFOLD DRAPE 41 X 57 PRODUCT NO. 900-633, RECORDER NO. 0633
K971920 GOWN POLY REINFORCED LARGE(PRODUCT NO.900-522)/(REORDER NO. 0522)
K964011 SUCTION CATHETER TRAY PRODUCT NO. 900277
K962596 CUSTOMED BLOOD EXTRACTION KIT
K961442 UNIVERSAL DRAINAGE TRAY
K953678 STERIMED STERIZATION WRAPPER (NON-STERILE)
K950295 WOUND CLOSURE/LACERATION TRAY
K942177 FOLEY CATHETERIZATION TRAY
K925018 IV PREP KIT W/O DRESSING (NON-STERILE)
K925017 IV PREP KIT (NON-STERILE)
Search all 36 clearances from Customed, Inc. →