This medical device record is a pma supplement. A supplement may have changed the device description/function or indication from that approved in the original pma. Be sure to look at the original pma record for more information.
Approval for the use of 100% ethylene oxide sterilization to be performed at medical manufacturing corporation, erie, pa
| Device | PAS LACROSSE TM PTCA CATHETER |
| Generic Name | Catheters, Transluminal Coronary Angioplasty, Percutaneous |
| Applicant | PROGRESSIVE ANGIOPLASTY SYSTEMS, INC. |
| Date Received | 1995-10-04 |
| Decision Date | 1996-04-02 |
| PMA | P930012 |
| Supplement | S001 |
| Product Code | LOX |
| Advisory Committee | Cardiovascular |
| Supplement Type | Normal 180 Day Track |
| Supplement Reason | Location Change - Manufacturer/sterilizer/packager/supplier |
| Expedited Review | No |
| Combination Product | No |
| Applicant Address | PROGRESSIVE ANGIOPLASTY SYSTEMS, INC. 1350 Willow Rd. Suite 201 menlo Park, CA 94025 |
| Supplement Number | Date | Supplement Type |
|---|---|---|
| P930012 | Original Filing | |
| S012 | 1998-07-24 | Normal 180 Day Track |
| S011 | 1998-08-03 | Real-time Process |
| S010 | 1998-05-08 | Real-time Process |
| S009 | 1998-01-08 | Real-time Process |
| S008 | 1997-08-19 | Normal 180 Day Track |
| S007 | ||
| S006 | 1997-03-06 | Normal 180 Day Track |
| S005 | 1996-08-01 | Normal 180 Day Track |
| S004 | 1996-06-27 | Normal 180 Day Track |
| S003 | 1995-11-13 | Normal 180 Day Track |
| S002 | 1995-10-04 | Normal 180 Day Track |
| S001 | 1995-10-04 | Normal 180 Day Track |