Atlas FDA

AngelMed Guardian System

FDA premarket approval P150009/S004 · decided 2020-12-22

Approval details

PMA number
P150009
Supplement
S004
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
AngelMed Guardian System
Generic name
Acute coronary syndrome event detector
Applicant
Avertix Medical, Inc.
Date received
2020-12-01
Decision date
2020-12-22
Days to decision
21 days
Decision code
OK30
Product code
QBI
Advisory committee
Cardiovascular
Expedited review
No
Location
Eatontown, NJ
Statement
component change the implantable and external device components of the AngelMed Guardian System

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