Medical Device Recalls
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1 result found
510(K) Number: K160951 |
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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 Efficia CMS200 Central Monitoring System; 863352 The Efficia CMS200 central monitoring syst... | 2 | 02/22/2017 | Philips Electronics North America Corporation |
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