FDA 510(k) FDA class 2 Substantially Equivalent 🇯🇵 Japan

ASAHI Corsair Microcatheter

K Number: K151103 · Decision Jun 23, 2015
Classifications
1
FEI Numbers
271
Registration Numbers
272
Same Product Code
880
Applicant Total
52
Review Days
60

Basic Information

Device Name
ASAHI Corsair Microcatheter
K Number
K151103
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1250
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
ASAHI INTECC CO., LTD.
Date Received
April 24, 2015
Decision Date
June 23, 2015
Product Code
DQY
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
DQY Catheter, Percutaneous

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