PMA P820018S051
- Device
- REFLEX MODEL 8223E DUAL CHAMBER PULSE GENERATOR
- Applicant
- St. Jude Medical, Inc.
- PMA number
- P820018
- Supplement
- S051
- Product code
- LWP
- Decision date
- 1991-10-25
- Generic name
- Implantable pulse generator, pacemaker (non-CRT)
Current openFDA PMA Record
- Device
- REFLEX MODEL 8223E DUAL CHAMBER PULSE GENERATOR
- Applicant
- St. Jude Medical, Inc.
- PMA number
- P820018
- Supplement
- S051
- Product code
- LWP
- Generic name
- Implantable pulse generator, pacemaker (non-CRT)
- Decision date
- 1991-10-25
- Decision code
- APPR
- Date received
- 1991-04-19
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Change Design/Components/Specifications/Material