Medical Device Recalls
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1 result found
510(K) Number: K934624 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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ACS Rotating Hemostatic Valve, .115 inch, for use with a dilatation catheter - Reference Number 2324... | 2 | 02/01/2007 | Abbott Vascular-Cardiac Therapies dba Guidant Corporation |
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