Medical Device Recalls
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1 result found
510(K) Number: K913471 |
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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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| ADAC ARGUS Gamma Camera Systems & ADAC CIRRUS Gamma Camera Systems. Distributed by Philips Medical ... | 2 | 01/17/2014 |
FEI # 1525965 Philips Medical Systems (Cleveland) Inc |
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