Medical Device Recalls
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1 result found
510(K) Number: K983373 |
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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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IMPACT Catheters, Balloon Dilatation and Esophageal Dilatation Catheter, Model Number 307, STERILE, ... | 2 | 12/15/2009 | Numed Inc |
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