Ventak P 1600 Aicd and 2830 Software Module

FDA premarket approval P890061 · Implantable cardioverter defibrillator (non-CRT)

PMA numberP890061

Approval

Applicant
Boston Scientific
Received
November 27, 1989
Decision date
May 2, 1991 (APPR)
Supplements
22, latest April 2, 2021
Product code
LWS – Implantable Cardioverter Defibrillator (Non-Crt)

Official FDA PMA record