FDA PMA FDA Class 3 Approved 🇺🇸 United States

Permanent Defibrillator Electrodes

PMA: P060039 · Supplement: S024 · Decision Jun 27, 2011
Classifications
1
FEI Numbers
36
Registration Numbers
36

Basic Information

Device Name
Permanent Defibrillator Electrodes
Trade Name
ATTAIN STARFIX LEAD
PMA Number
P060039
Supplement Number
S024
Device Class
FDA Class 3
Product Code
NVY
Generic Name
Permanent defibrillator electrodes
Medical Specialty
Unknown
Advisory Committee
Cardiovascular
Decision
Approved
Decision Code
APPR
Decision Date
June 27, 2011
Date Received
March 22, 2011
Supplement Type
135 Review Track For 30-Day Notice
Supplement Reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review
N

Advisory Committee Statement

APPROVAL FOR THE CHANGE OF THE CLEANING CONTROL AREA AND THE ASSOCIATED PROCESSES.

Classifications

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

Product Code Device Name
NVY Permanent Defibrillator Electrodes