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PARADYM VR 8750,PARADYM DR8750,ISOLINE 2CT-ISOLINE 2CR

FDA premarket approval P980049/S087 · decided 2013-10-02

Approval details

PMA number
P980049
Supplement
S087
Supplement type
30-Day Notice
Trade name
PARADYM VR 8750,PARADYM DR8750,ISOLINE 2CT-ISOLINE 2CR
Generic name
DEFIBRILLATOR, IMPLANTABLE, DUAL-CHAMBER
Applicant
MicroPort CRM USA, Inc.
Date received
2013-09-11
Decision date
2013-10-02
Days to decision
21 days
Decision code
OK30
Product code
MRM
Advisory committee
Cardiovascular
Expedited review
No
Location
Arlington, TN
Statement
CHANGE TO THE ROUTINE BIOBURDEN MONITORING BEFORE STERILIZATION.

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