FDA PMA FDA Class 3 Approved 🇺🇸 United States

Pacemaker/Icd/Crt Non-Implanted Components

PMA: P890003 · Supplement: S344 · Decision Feb 5, 2016
Classifications
1
FEI Numbers
34
Registration Numbers
34

Basic Information

Device Name
Pacemaker/Icd/Crt Non-Implanted Components
Trade Name
MEDTRONIC CARELINK MONITOR, MYCARELINK PATIENT MONITOR
PMA Number
P890003
Supplement Number
S344
Device Class
FDA Class 3
Product Code
OSR
Generic Name
Pacemaker/icd/crt non-implanted components
Medical Specialty
Unknown
Advisory Committee
Cardiovascular
Decision
Approved
Decision Code
APPR
Decision Date
February 5, 2016
Date Received
November 16, 2015
Supplement Type
Normal 180 Day Track
Supplement Reason
Change Design/Components/Specifications/Material
Expedited Review
N

Advisory Committee Statement

Approval for the Alert Management Feature for the CareLink Network.

Classifications

This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.

Product Code Device Name
OSR Pacemaker/Icd/Crt Non-Implanted Components