PMA P870043S013
- Device
- MODEL 1210 OMNIPULSE(TM) HOLMIUM LASER SYSTEM
- Applicant
- Trimedyne, Inc.
- PMA number
- P870043
- Supplement
- S013
- Product code
- LPC
- Decision date
- 1991-08-20
- Classification
- Device, Angioplasty, Laser, Coronary
- Generic name
- DEVICE, ANGIOPLASTY, LASER, CORONARY
Current openFDA PMA Record#
- Device
- MODEL 1210 OMNIPULSE(TM) HOLMIUM LASER SYSTEM
- Applicant
- Trimedyne, Inc.
- PMA number
- P870043
- Supplement
- S013
- Product code
- LPC
- Generic name
- DEVICE, ANGIOPLASTY, LASER, CORONARY
- Decision date
- 1991-08-20
- Decision code
- APPR
- Date received
- 1990-12-06
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Change Design/Components/Specifications/Material