PMA P890032S020
- Device
- CORDIS ORION STEERABLE PTCA BALLOON CATHETER
- Applicant
- Cordis Corp.
- PMA number
- P890032
- Supplement
- S020
- Product code
- LOX
- Decision date
- 1995-04-27
- Generic name
- Catheters, transluminal coronary angioplasty, percutaneous
Current openFDA PMA Record
- Device
- CORDIS ORION STEERABLE PTCA BALLOON CATHETER
- Applicant
- Cordis Corp.
- PMA number
- P890032
- Supplement
- S020
- Product code
- LOX
- Generic name
- Catheters, transluminal coronary angioplasty, percutaneous
- Decision date
- 1995-04-27
- Decision code
- APPR
- Date received
- 1995-03-16
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Labeling Change - Indications/instructions/shelf life/tradename