PMA P880003S025
- Device
- Cordis Ptca Dilitation Cartheters
- Applicant
- CORDIS CORP.
- PMA number
- P880003
- Supplement
- S025
- Decision date
- 1995-08-04
Current openFDA PMA Record
- Device
- CORDIS PTCA DILITATION CARTHETERS
- Applicant
- Cordis Corp.
- PMA number
- P880003
- Supplement
- S025
- Product code
- LOX
- Generic name
- Catheters, transluminal coronary angioplasty, percutaneous
- Decision date
- 1995-08-04
- Decision code
- APPR
- Date received
- 1993-12-06
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Location Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- APPROVAL FOR ALTERNATE STERILIZATION SITE AND ELIMINATION OF CHLOROFLUOROCARBONS (CFC'S) FROM THE STERILIZATION PROCESS