Medical Device Recalls
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1 result found
510(K) Number: K901627 |
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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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Embolectomy Catheters (Models A44XX, A4FXX, CE0XXXST, and CE0XXX): Model Numbers & Description: ... | 2 | 09/25/2012 | Applied Medical Resources Corp |
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