PMA P910001S127
- Device
- Philips Laser System
- Applicant
- Spectranetics Corp.
- PMA number
- P910001
- Supplement
- S127
- Product code
- LPC
- Decision date
- 2026-08-21
- Classification
- Cardiovascular
- Generic name
- DEVICE, ANGIOPLASTY, LASER, CORONARY
- Approval order statement
- the implementation of a secondary supplier for cable assemblies
Current openFDA PMA Record#
- Device
- Philips Laser System
- Applicant
- Spectranetics Corp.
- PMA number
- P910001
- Supplement
- S127
- Product code
- LPC
- Generic name
- DEVICE, ANGIOPLASTY, LASER, CORONARY
- Decision date
- 2026-08-21
- Decision code
- OK30
- Date received
- 2026-07-23
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- the implementation of a secondary supplier for cable assemblies