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

PLASTIC LEG BAG

K Number: K831530 · Decision Jan 3, 1984
Classifications
1
FEI Numbers
127
Registration Numbers
127
Same Product Code
205
Applicant Total
1
Review Days
236

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Basic Information

Device Name
PLASTIC LEG BAG
K Number
K831530
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5250
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Forever-Dry, Inc.
Date Received
May 12, 1983
Decision Date
January 3, 1984
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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