Medical Device Recalls
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1 result found
510(K) Number: K133125 |
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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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Nokia BPM+ Wireless Blood Pressure Monitor Product System, measurement, blood-pressure, non-inva... | 2 | 08/16/2018 | Withings Sas |
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