PMA P880006S009
- Device
- SENSOLOG III MODEL 2033B & DIALOG II MODEL 2037B
- Applicant
- St. Jude Medical, Inc.
- PMA number
- P880006
- Supplement
- S009
- Product code
- DXY
- Decision date
- 1993-01-11
- Generic name
- implantable pacemaker Pulse-generator
- Approval order statement
- APPROVAL FOR RELOCATING THE MANUFACTURING FACILITIES TO 15900 VALLEYVIEW COURT, SYLMAR, CA., 91392-9221
Current openFDA PMA Record
- Device
- SENSOLOG III MODEL 2033B & DIALOG II MODEL 2037B
- Applicant
- St. Jude Medical, Inc.
- PMA number
- P880006
- Supplement
- S009
- Product code
- DXY
- Generic name
- implantable pacemaker Pulse-generator
- Decision date
- 1993-01-11
- Decision code
- APPR
- Date received
- 1991-03-29
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Location Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- APPROVAL FOR RELOCATING THE MANUFACTURING FACILITIES TO 15900 VALLEYVIEW COURT, SYLMAR, CA., 91392-9221