This medical device has supplements. The device description/function or indication may have changed. Be sure to look at the supplements to get an up-to-date information on device changes. The labeling included below is the version at time of approval of the original pma or panel track supplement and may not represent the most recent labeling.
| Device | ORACLE(TM) CORONARY BALLOON DILATATION CATHETER |
| Generic Name | Catheters, Transluminal Coronary Angioplasty, Percutaneous |
| Applicant | ABBOTT VASCULAR DEVICES |
| Date Received | 1991-06-07 |
| Decision Date | 1994-09-30 |
| Notice Date | 1994-12-15 |
| PMA | P910031 |
| Supplement | S |
| Product Code | LOX |
| Docket Number | 94M-0402 |
| Advisory Committee | Cardiovascular |
| Expedited Review | No |
| Combination Product | No |
| Applicant Address | ABBOTT VASCULAR DEVICES 400 Saginaw Dr. redwood City, CA 94063 |
| Supplement Number | Date | Supplement Type |
|---|---|---|
| P910031 | Original Filing | |
| S026 | 2009-07-29 | 30-day Notice |
| S025 | ||
| S024 | 2007-05-04 | Normal 180 Day Track No User Fee |
| S023 | 2004-11-16 | Normal 180 Day Track |
| S022 | 2004-11-01 | Normal 180 Day Track |
| S021 | 2001-12-06 | Normal 180 Day Track |
| S020 | ||
| S019 | 1998-06-15 | Normal 180 Day Track |
| S018 | ||
| S017 | 1997-10-14 | Real-time Process |
| S016 | 1997-05-22 | Real-time Process |
| S015 | 1997-03-28 | Normal 180 Day Track |
| S014 | ||
| S013 | ||
| S012 | 1996-09-30 | Normal 180 Day Track |
| S011 | 1996-08-26 | Normal 180 Day Track |
| S010 | 1996-07-23 | Normal 180 Day Track |
| S009 | 1996-05-15 | Normal 180 Day Track |
| S008 | 1996-02-09 | Normal 180 Day Track |
| S007 | 1996-01-26 | Normal 180 Day Track |
| S006 | 1995-11-03 | Normal 180 Day Track |
| S005 | 1995-09-07 | Normal 180 Day Track |
| S004 | 1995-08-18 | Normal 180 Day Track |
| S003 | 1995-06-02 | Normal 180 Day Track |
| S002 | 1995-03-30 | Normal 180 Day Track |
| S001 | 1994-11-21 | Normal 180 Day Track |