PMA P880086S040
- Device
- TRILOGY DC + PULSE GENERATOR, MODEL 2318L
- Applicant
- ABBOTT MEDICAL
- PMA number
- P880086
- Supplement
- S040
- Product code
- DXY
- Decision date
- 1997-01-10
- Classification
- Implantable Pacemaker Pulse-generator
- Generic name
- implantable pacemaker Pulse-generator
- Approval order statement
- APPROVAL FOR THE TRILOGY DC+ MODEL 2318L PULSE GENERATOR WITH MODEL 3204A FUNCTION PACK FOR USE WITH THE APS II MODEL 30003 PROGRAMMER.
Current openFDA PMA Record#
- Device
- TRILOGY DC + PULSE GENERATOR, MODEL 2318L
- Applicant
- ABBOTT MEDICAL
- PMA number
- P880086
- Supplement
- S040
- Product code
- DXY
- Generic name
- implantable pacemaker Pulse-generator
- Decision date
- 1997-01-10
- Decision code
- APPR
- Date received
- 1996-11-08
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Change Design/Components/Specifications/Material
- Approval order statement
- APPROVAL FOR THE TRILOGY DC+ MODEL 2318L PULSE GENERATOR WITH MODEL 3204A FUNCTION PACK FOR USE WITH THE APS II MODEL 30003 PROGRAMMER.