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CARPENTIER-EDWARDS PERIMOUNT PERICARDFIAL AORTIC BIOPROSTHESIS

FDA premarket approval P860057/S124 · decided 2014-05-13

Approval details

PMA number
P860057
Supplement
S124
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
CARPENTIER-EDWARDS PERIMOUNT PERICARDFIAL AORTIC BIOPROSTHESIS
Generic name
replacement Heart-valve
Applicant
Edwards Lifesciences, LLC
Date received
2014-04-15
Decision date
2014-05-13
Days to decision
28 days
Decision code
OK30
Product code
DYE
Advisory committee
Cardiovascular
Expedited review
No
Location
Irvine, CA
Statement
UPGRADE OF THE VALVE FLOW AND LEAFLET COAPTATION TESTER.

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Hypertension Prediction Index (HePI) Algorithm (K242518)Edwards Lifesciences, LLC2025-05-15
FloTrac sensors; FloTrac Jr sensors; Acumen IQ sensors; VolumeView sensors (K242909)Edwards Lifesciences, LLC2025-03-21
Fogarty Thru-Lumen Embolectomy Catheter (K240078)Edwards Lifesciences, LLC2024-08-28
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