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

SMALL CATHETER INFLATOR

K Number: K896005 · Decision Feb 26, 1990
Classifications
1
FEI Numbers
64
Registration Numbers
64
Same Product Code
56
Applicant Total
1
Review Days
136

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Basic Information

Device Name
SMALL CATHETER INFLATOR
K Number
K896005
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1650
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Allied Systems Co.
Date Received
October 13, 1989
Decision Date
February 26, 1990
Product Code
MAV
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MAV Syringe, Balloon Inflation

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