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

VAPRO INTERMITTENT CATHETER, MODEL 72062, 72082,72102, 72122, 72142, 72064, 72084, 72104, 72124,72144, 72164, 72184,

K Number: K090960 · Decision Aug 20, 2009
Classifications
1
FEI Numbers
83
Registration Numbers
83
Same Product Code
70
Applicant Total
85
Review Days
136

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Basic Information

Device Name
VAPRO INTERMITTENT CATHETER, MODEL 72062, 72082,72102, 72122, 72142, 72064, 72084, 72104, 72124,72144, 72164, 72184,
K Number
K090960
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5130
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Hollister, Inc.
Date Received
April 6, 2009
Decision Date
August 20, 2009
Product Code
GBM
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
GBM Catheter, Urethral

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