PMA P940008S014
- Device
- IMPLANTABLE PACEMAKER LEAD
- Applicant
- Boston Scientific
- PMA number
- P940008
- Supplement
- S014
- Decision date
- 1999-12-02
- Approval order statement
- Approval for the manufacturing and labeling facility located at Guidant Corp., St. Paul, MN 55112-5798.
Current openFDA PMA Record
- Device
- IMPLANTABLE PACEMAKER LEAD
- Applicant
- Boston Scientific
- PMA number
- P940008
- Supplement
- S014
- Decision date
- 1999-12-02
- Decision code
- APPR
- Date received
- 1999-10-25
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Express GMP Supplement
- Approval order statement
- Approval for the manufacturing and labeling facility located at Guidant Corp., St. Paul, MN 55112-5798.