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

4 SURE URINARY DRAIN BAG

K Number: K896727 · Decision Feb 20, 1990
Classifications
1
FEI Numbers
127
Registration Numbers
127
Same Product Code
205
Applicant Total
4
Review Days
83

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Basic Information

Device Name
4 SURE URINARY DRAIN BAG
K Number
K896727
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5250
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
The Boston & Pacific Co., Inc.
Date Received
November 29, 1989
Decision Date
February 20, 1990
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (KNX), ordered by most recent decision date.

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Other Clearances by The Boston & Pacific Co., Inc.

K Number Device Name
K896726 4 SURE EXTERNAL MALE CATHETER
K896728 4 SURE URINARY LEG BAG
K896725 4 SURE UROLOGICAL CATHETER