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

ARCHER SUPER STIFF GUIDEWIRES

K Number: K101339 · Decision Aug 31, 2010
Classifications
1
FEI Numbers
252
Registration Numbers
253
Same Product Code
751
Applicant Total
84
Review Days
111

Basic Information

Device Name
ARCHER SUPER STIFF GUIDEWIRES
K Number
K101339
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1330
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
MEDTRONIC INC.
Date Received
May 12, 2010
Decision Date
August 31, 2010
Product Code
DQX
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
DQX Wire, Guide, Catheter

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