Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K151520 |
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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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Oscar 2, Model 250 System | 2 | 06/25/2020 | Suntech Medical, Inc. |
Model 250D Ambulatory Blood Pressure Monitor labeled under the following brands: Bravo Mini, part n... | 2 | 01/14/2020 | Suntech Medical, Inc. |
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