FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

URINARY GEL DRAINAGE SYSTEM

K Number: K952780 · Decision Dec 12, 1995
Classifications
1
FEI Numbers
49
Registration Numbers
49
Same Product Code
13
Applicant Total
1
Review Days
179

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Basic Information

Device Name
URINARY GEL DRAINAGE SYSTEM
K Number
K952780
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
876.5250
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
P.A.M., Inc.
Date Received
June 16, 1995
Decision Date
December 12, 1995
Product Code
EYZ
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
EYZ System, Urine Drainage, Closed, For Nonindwelling Catheter, Sterile

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