PMA P850021S030
- Device
- Hybrid (ptca) Catheter
- Applicant
- ABBOTT VASCULAR INC.
- PMA number
- P850021
- Supplement
- S030
- Decision date
- 1995-07-12
Current openFDA PMA Record
- Device
- HYBRID (PTCA) CATHETER
- Applicant
- Abbott Vascular, Inc.
- PMA number
- P850021
- Supplement
- S030
- Product code
- LOX
- Generic name
- Catheters, transluminal coronary angioplasty, percutaneous
- Decision date
- 1995-07-12
- Decision code
- APPR
- Date received
- 1995-03-09
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Location Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- APPROVAL FOR A MANUFACTURING MODIFICATION TO THE INNER BODY OF THE ABOVE CATHETERS