PMA P820018S072
- Device
- MODEL 9602 PROGRAMMER
- Applicant
- St. Jude Medical, Inc.
- PMA number
- P820018
- Supplement
- S072
- Product code
- LWP
- Decision date
- 1997-04-29
- Generic name
- Implantable pulse generator, pacemaker (non-CRT)
- Approval order statement
- ALTERNATE MANUFACTURING SITE FOR THE MODEL 9602 PROGRAMMER. THE SITE IS LOCATED AT PACESETTER, INC., 15900 VALLEY VIEW CT., SYLMAR, CA.
Current openFDA PMA Record
- Device
- MODEL 9602 PROGRAMMER
- Applicant
- St. Jude Medical, Inc.
- PMA number
- P820018
- Supplement
- S072
- Product code
- LWP
- Generic name
- Implantable pulse generator, pacemaker (non-CRT)
- Decision date
- 1997-04-29
- Decision code
- APPR
- Date received
- 1997-04-24
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Location Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- ALTERNATE MANUFACTURING SITE FOR THE MODEL 9602 PROGRAMMER. THE SITE IS LOCATED AT PACESETTER, INC., 15900 VALLEY VIEW CT., SYLMAR, CA.