Guidant Corporation ACS
3 FDA 510(k) clearances · Recalling firm
◉ Watch Guidant Corporation ACS
| Record | Firm | Date |
|---|---|---|
| Guidant Multi-Link Zeta Coronary Stent System recall (Z-1075-03) | Guidant Corporation ACS | 2003-08-01 |
| MULTI-LINK Pixel Coronary Stent System Size: 2.0 x 13 mm OTW Part Number: 1007830-13 recall (Z-0862-03) | Guidant Corporation ACS | 2003-05-22 |
| Guidant Multi-Link Vision Coronary Stent System Catalog Numbers: 30 different catalog numb recall (Z-0775-03) | Guidant Corporation ACS | 2003-04-22 |
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Every clearance here is in the API, with alerts when new ones post.