PMA P890032S001
- Device
- Angioplasty (ptca) Dilatation Catheters
- Applicant
- CORDIS CORP.
- PMA number
- P890032
- Supplement
- S001
- Decision date
- 1990-04-30
Current openFDA PMA Record
- Device
- ANGIOPLASTY (PTCA) DILATATION CATHETERS
- Applicant
- Cordis Corp.
- PMA number
- P890032
- Supplement
- S001
- Product code
- LOX
- Generic name
- Catheters, transluminal coronary angioplasty, percutaneous
- Decision date
- 1990-04-30
- Decision code
- APPR
- Date received
- 1990-03-12
- Supplement type
- Special (Immediate Track)
- Supplement reason
- Labeling Change - Indications/instructions/shelf life/tradename