Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K010341 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| MurphyScope, Bayonet, Malleable, Catalog # 2121-157 | 3 | 03/12/2005 |
FEI # 3015531529 Medtronic Neurosurgery |
| MurphyScope, Curved, Mallaeble, Catalog # 2125-163 | 3 | 03/12/2005 |
FEI # 3015531529 Medtronic Neurosurgery |
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