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

WILDCAT 5F GUIDEWIRE SUPPORT CATHETER

K Number: K112579 · Decision Oct 6, 2011
Classifications
1
FEI Numbers
276
Registration Numbers
277
Same Product Code
889
Applicant Total
25
Review Days
30

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Basic Information

Device Name
WILDCAT 5F GUIDEWIRE SUPPORT CATHETER
K Number
K112579
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
870.1250
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Avinger, Inc.
Date Received
September 6, 2011
Decision Date
October 6, 2011
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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