PMA P880086S036

Device: TRILOGY DR+ PULSE GENERATOR MODELS 2360L AND 2364L PULSE GENERATORS MODELS 2360L AND 2364L
Applicant: ABBOTT MEDICAL
PMA number: P880086
Supplement: S036
Product code: DXY
Decision date: 1996-09-30
Classification: Implantable Pacemaker Pulse-generator
Generic name: implantable pacemaker Pulse-generator
Approval order statement: APPROVAL FOR THE TRILOGY DR+ PACING SYSTEM INCLUDING MODELS 2360L AND 2364L, AND THE MODEL 3203A FUNCTION PACK

Current openFDA PMA Record#

Device: TRILOGY DR+ PULSE GENERATOR MODELS 2360L AND 2364L PULSE GENERATORS MODELS 2360L AND 2364L
Applicant: ABBOTT MEDICAL
PMA number: P880086
Supplement: S036
Product code: DXY
Generic name: implantable pacemaker Pulse-generator
Decision date: 1996-09-30
Decision code: APPR
Date received: 1996-03-21
Supplement type: Normal 180 Day Track
Supplement reason: Change Design/Components/Specifications/Material
Approval order statement: APPROVAL FOR THE TRILOGY DR+ PACING SYSTEM INCLUDING MODELS 2360L AND 2364L, AND THE MODEL 3203A FUNCTION PACK