Medical Device Recalls
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1 result found
510(K) Number: K945633 |
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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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| Channel Neuroendoscope, Standard Resolution, 21.6 cm. Catalog No. 2232-001 | 3 | 07/20/2004 |
FEI # 3015531529 Medtronic Neurosurgery |
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