Medical Device Recalls
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1 result found
510(K) Number: K924593 |
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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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Diagnost 56/66/76/76 Plus, DSI is a Spot-Film and has a Digital Imaging Spot. Intended use is for... | 2 | 09/13/2010 | Philips Medical Systems North America Co. Phillips |
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