PMA P890032S014
- Device
- CORDIS ORION II STEERABLE BALLOON CATHETER
- Applicant
- Cordis Corp.
- PMA number
- P890032
- Supplement
- S014
- Product code
- LOX
- Decision date
- 1993-06-17
- Generic name
- Catheters, transluminal coronary angioplasty, percutaneous
Current openFDA PMA Record
- Device
- CORDIS ORION II STEERABLE BALLOON CATHETER
- Applicant
- Cordis Corp.
- PMA number
- P890032
- Supplement
- S014
- Product code
- LOX
- Generic name
- Catheters, transluminal coronary angioplasty, percutaneous
- Decision date
- 1993-06-17
- Decision code
- APPR
- Date received
- 1992-02-24
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Change Design/Components/Specifications/Material