PMA P860007S010
- Device
- INTERTACH(R)II MODELS 262-16/262-16R DISCON.TEST
- Applicant
- Boston Scientific
- PMA number
- P860007
- Supplement
- S010
- Product code
- LWW
- Decision date
- 1993-01-11
- Generic name
- PULSE-GENERATOR, SINGLE CHAMBER, SINGLE
Current openFDA PMA Record
- Device
- INTERTACH(R)II MODELS 262-16/262-16R DISCON.TEST
- Applicant
- Boston Scientific
- PMA number
- P860007
- Supplement
- S010
- Product code
- LWW
- Generic name
- PULSE-GENERATOR, SINGLE CHAMBER, SINGLE
- Decision date
- 1993-01-11
- Decision code
- APPR
- Date received
- 1992-07-10
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Change Design/Components/Specifications/Material