FDA PMA FDA Class 3 30-Day Notice Accepted 🇺🇸 United States

Ventricular (Assist) Bypass

PMA: P160035 · Supplement: S012 · Decision Nov 3, 2019
Classifications
1
FEI Numbers
21
Registration Numbers
21

Basic Information

Device Name
Ventricular (Assist) Bypass
Trade Name
Excor Pediatric Ventricular Assist Device
PMA Number
P160035
Supplement Number
S012
Device Class
FDA Class 3
Product Code
DSQ
Generic Name
Ventricular (assist) bypass
Medical Specialty
Unknown
Advisory Committee
Cardiovascular
Decision
30-Day Notice Accepted
Decision Code
OK30
Decision Date
November 3, 2019
Date Received
October 11, 2019
Supplement Type
30-Day Notice
Supplement Reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review
N

Advisory Committee Statement

Raise the comparator threshold value for buzzer board for IKUS driver.

Classifications

This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DSQ Ventricular (Assist) Bypass