Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K854261 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| ACS DUOSTAT® Rotating Hemostatic Valve, 0.096 inch, for use with a dilatation catheter - Reference ... | 2 | 02/01/2007 | Abbott Vascular-Cardiac Therapies dba Guidant Corporation |
| ACS Rotating Hemostatic Valve, 0.096 inch, for use with a dilatation catheter - Reference Number 232... | 2 | 02/01/2007 | Abbott Vascular-Cardiac Therapies dba Guidant Corporation |
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