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

Confirm Rx Insertable Cardiac Monitor

K Number: K192593 · Decision Oct 18, 2019
Classifications
1
FEI Numbers
6
Registration Numbers
6
Same Product Code
22
Applicant Total
12
Review Days
28

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Basic Information

Device Name
Confirm Rx Insertable Cardiac Monitor
K Number
K192593
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
870.2800
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Abbott
Date Received
September 20, 2019
Decision Date
October 18, 2019
Product Code
MXC
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
MXC Recorder, Event, Implantable Cardiac, (Without Arrhythmia Detection)

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