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

VEIN VALVE CUTTER

K Number: K862724 · Decision Jan 2, 1987
Classifications
1
FEI Numbers
276
Registration Numbers
277
Same Product Code
889
Applicant Total
89
Review Days
169

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Basic Information

Device Name
VEIN VALVE CUTTER
K Number
K862724
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1250
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
American Edwards Laboratories
Date Received
July 17, 1986
Decision Date
January 2, 1987
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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