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

Torqr Intracardiac Electrode Catheter, Soloist Intracardiac Electrode Catheter

K Number: K190132 · Decision Jul 30, 2019
Classifications
1
FEI Numbers
86
Registration Numbers
86
Same Product Code
182
Applicant Total
30
Review Days
183

Basic Information

Device Name
Torqr Intracardiac Electrode Catheter, Soloist Intracardiac Electrode Catheter
K Number
K190132
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1220
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medtronic
Date Received
January 28, 2019
Decision Date
July 30, 2019
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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