FDA PMA FDA Class 3 Approved 🇺🇸 United States

Over-The-Counter Automated External Defibrillator

PMA: P160029 · Supplement: S019 · Decision Apr 3, 2023
Classifications
1
FEI Numbers
8
Registration Numbers
8

Basic Information

Device Name
Over-The-Counter Automated External Defibrillator
Trade Name
HeartStart OnSite Defibrillator (Model M5066A) and HeartStart Home Defibrillator (Model M5068A)
PMA Number
P160029
Supplement Number
S019
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
Approved
Decision Code
APPR
Decision Date
April 3, 2023
Date Received
January 3, 2023
Supplement Type
Real-Time Process
Supplement Reason
Change Design/Components/Specifications/Material
Expedited Review
N

Advisory Committee Statement

Approval for design changes including hardware changes for compliance with international restricted material regulations.

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