Medical Device Recalls
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1 result found
510(K) Number: K120212 |
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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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Brand Name: AFX" Introducer System, Model Number S17-45. Lot Numbers: 1079840, 1079843, 1079844, 10... | 1 | 06/07/2013 | Endologix Inc |
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