Atlas FDA

MYCARELINK PATIENT MONITOR

FDA premarket approval P890003/S306 · decided 2014-05-23

Approval details

PMA number
P890003
Supplement
S306
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
MYCARELINK PATIENT MONITOR
Generic name
Pulse generator, permanent, implantable
Applicant
Medtronic, Inc.
Date received
2014-03-28
Decision date
2014-05-23
Days to decision
56 days
Decision code
APPR
Product code
NVZ
Advisory committee
Cardiovascular
Expedited review
No
Location
Mounds View, MN
Statement
APPROVAL FOR FIRMWARE UPDATES TO THE MYCARELINK PATIENT MONITOR24950.

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