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

FOGARTY VALVULOTOME, MODEL 700091

K Number: K001734 · Decision Mar 26, 2001
Classifications
1
FEI Numbers
12
Registration Numbers
12
Same Product Code
25
Applicant Total
77
Review Days
292

Basic Information

Device Name
FOGARTY VALVULOTOME, MODEL 700091
K Number
K001734
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.4885
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
EDWARDS LIFESCIENCES, LLC.
Date Received
June 7, 2000
Decision Date
March 26, 2001
Product Code
MGZ
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
MGZ Valvulotome

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