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LUMAX 300 DR-T/LUMAX 340 DR-T,LUMAX 300 VR-T/LUMAX 340 VR-T,LUMAX 500 DR-T/LUMAX 540 DR-T,LUMAX 500 VR-T/LUMAX 540 VR-T,

FDA premarket approval P050023/S063 · decided 2013-05-08

Approval details

PMA number
P050023
Supplement
S063
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
LUMAX 300 DR-T/LUMAX 340 DR-T,LUMAX 300 VR-T/LUMAX 340 VR-T,LUMAX 500 DR-T/LUMAX 540 DR-T,LUMAX 500 VR-T/LUMAX 540 VR-T,
Generic name
DEFIBRILLATOR, IMPLANTABLE, DUAL-CHAMBER
Applicant
Biotronik, Inc.
Date received
2013-04-03
Decision date
2013-05-08
Days to decision
35 days
Decision code
APPR
Product code
MRM
Advisory committee
Cardiovascular
Expedited review
No
Location
Lake Oswego, OR
Statement
APPROVAL FOR THE UPDATED VERSION 3.22.0 OF HOME MONITORINGSERVICE CENTER INCLUDING THE FEATURES:1) IMPLEMENTATION OF REMOTE SCHEDULING; AND2) AUTOMATIC EXPORT OF EHR DATA.

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510(k) clearances by this applicant

RecordFirmDate
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