PMA P880086S033
- Device
- TRILOGY PULSE GENERATOR MODELS 235OL, 2250L, AND 2308L
- Applicant
- ABBOTT MEDICAL
- PMA number
- P880086
- Supplement
- S033
- Product code
- DXY
- Decision date
- 1995-11-01
- Classification
- Implantable Pacemaker Pulse-generator
- Generic name
- implantable pacemaker Pulse-generator
- Approval order statement
- APPROVAL FOR ALTERNATIVE HYBRID SUBSTRATE
Current openFDA PMA Record#
- Device
- TRILOGY PULSE GENERATOR MODELS 235OL, 2250L, AND 2308L
- Applicant
- ABBOTT MEDICAL
- PMA number
- P880086
- Supplement
- S033
- Product code
- DXY
- Generic name
- implantable pacemaker Pulse-generator
- Decision date
- 1995-11-01
- Decision code
- APPR
- Date received
- 1995-08-02
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Change Design/Components/Specifications/Material
- Approval order statement
- APPROVAL FOR ALTERNATIVE HYBRID SUBSTRATE