PMA P850021S025
- Device
- Hybrid (ptca) Catheter
- Applicant
- ABBOTT VASCULAR INC.
- PMA number
- P850021
- Supplement
- S025
- Decision date
- 1994-07-26
Current openFDA PMA Record
- Device
- HYBRID (PTCA) CATHETER
- Applicant
- Abbott Vascular, Inc.
- PMA number
- P850021
- Supplement
- S025
- Product code
- LOX
- Generic name
- Catheters, transluminal coronary angioplasty, percutaneous
- Decision date
- 1994-07-26
- Decision code
- APPR
- Date received
- 1993-12-20
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Change Design/Components/Specifications/Material