Medical Device Recalls
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1 result found
510(K) Number: K161937 |
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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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CuattroDR System Software, REF: SWR-00069-MD, UDI: B269SWR00069MD0 | 2 | 05/08/2020 | Cuattro LLC |
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