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

ACHIEVE MAPPING CATHETER AND ELECTRICAL CABLE

K Number: K102588 · Decision Mar 18, 2011
Classifications
1
FEI Numbers
88
Registration Numbers
88
Same Product Code
184
Applicant Total
1
Review Days
190

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Basic Information

Device Name
ACHIEVE MAPPING CATHETER AND ELECTRICAL CABLE
K Number
K102588
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1220
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medtronic Ablation Frontiers, LLC
Date Received
September 9, 2010
Decision Date
March 18, 2011
Product Code
DRF
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
DRF Catheter, Electrode Recording, Or Probe, Electrode Recording

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