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

Over-The-Counter Automated External Defibrillator

PMA: P160029 · Supplement: S015 · Decision Mar 20, 2022
Classifications
1
FEI Numbers
8
Registration Numbers
8

Basic Information

Device Name
Over-The-Counter Automated External Defibrillator
Trade Name
HeartStart OnSite Home Defibrillator
PMA Number
P160029
Supplement Number
S015
Device Class
FDA Class 3
Product Code
NSA
Generic Name
Over-the-counter automated external defibrillator
Regulation Number
870.5310
Medical Specialty
Cardiovascular
Advisory Committee
Cardiovascular
Decision
30-Day Notice Accepted
Decision Code
OK30
Decision Date
March 20, 2022
Date Received
February 22, 2022
Supplement Type
30-Day Notice
Supplement Reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review
N

Advisory Committee Statement

an alternate supplier for the high voltage capacitor used for the HS1 and FRx devices

Classifications

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

Product Code Device Name
NSA Over-The-Counter Automated External Defibrillator