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

BESECURE EXTERNAL URINARY COLLECTION SYSTEM

K Number: K971271 · Decision Aug 18, 1997
Classifications
1
FEI Numbers
127
Registration Numbers
127
Same Product Code
205
Applicant Total
1
Review Days
136

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Basic Information

Device Name
BESECURE EXTERNAL URINARY COLLECTION SYSTEM
K Number
K971271
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5250
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Urology Research Intl., Inc.
Date Received
April 4, 1997
Decision Date
August 18, 1997
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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