FDA PMA FDA Class 3 Approved 🇺🇸 United States

Programmer, Pacemaker

PMA: P880006 · Supplement: S032 · Decision Jun 26, 2000
Classifications
1
FEI Numbers
22
Registration Numbers
22

Basic Information

Device Name
Programmer, Pacemaker
Trade Name
MODEL 3307 V1.2A PROGRAMMER SOFTWARE FOR THE MODEL 3500/3510 PROGRAMMERS
PMA Number
P880006
Supplement Number
S032
Device Class
FDA Class 3
Product Code
KRG
Generic Name
Programmer, pacemaker
Regulation Number
870.3700
Medical Specialty
Cardiovascular
Advisory Committee
Cardiovascular
Decision
Approved
Decision Code
APPR
Decision Date
June 26, 2000
Date Received
May 25, 2000
Supplement Type
Real-Time Process
Supplement Reason
Change Design/Components/Specifications/Material
Expedited Review
N

Advisory Committee Statement

APPROVAL FOR MODEL 3307 V1.2A PROGRAMMER SOFTWARE FOR THE MODEL 3500/3510 PROGRAMMERS.

Classifications

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

Product Code Device Name
KRG Programmer, Pacemaker