Medical Device Recalls
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1 result found
510(K) Number: K051351 |
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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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Precedence SPECT/CT System, Precedence 16 3/8, Upper Patient Pallet, A single photon nuclear medicin... | 2 | 01/12/2011 | Phillips Nuclear Medicine |
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