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CARPENTER-EDWARDS PERIMOUNT BIOPROSTHESIS HEART VALVE FAMILIES

FDA premarket approval P860057/S134 · decided 2015-04-16

Approval details

PMA number
P860057
Supplement
S134
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
CARPENTER-EDWARDS PERIMOUNT BIOPROSTHESIS HEART VALVE FAMILIES
Generic name
replacement Heart-valve
Applicant
Edwards Lifesciences, LLC
Date received
2015-03-17
Decision date
2015-04-16
Days to decision
30 days
Decision code
OK30
Product code
DYE
Advisory committee
Cardiovascular
Expedited review
No
Location
Irvine, CA
Statement
RELOCATION OF THE SUPPLIER OF THE 3.8 OUNCE PACKAGING JARS USED FOR SURGICAL AND TRANSCATHETER HEART VALVES.

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510(k) clearances by this applicant

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Respiration Rate algorithm (K251326)Edwards Lifesciences, LLC2026-06-11
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Carpentier-Edwards Physio Annuloplasty Ring (4450) (K251688)Edwards Lifesciences, LLC2025-09-17
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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