Medical Device Recalls
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1 result found
510(K) Number: K111083 |
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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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Philips Avalon Monitors with software revision J.30.58: Model Product FM20 M2702A ; FM30 M2... | 2 | 10/21/2014 | Philips Medical Systems, Inc. |
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