Medical Device Recalls
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1 result found
510(K) Number: K914807 |
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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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| Elscint APEX Helix, dual-head, multi-purpose, Slip-Ring, digital gamma camera Product Usage: Th... | 1 | 07/24/2013 |
FEI # 2126677 GE Healthcare, LLC |
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