Medical Device Recalls
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1 result found
510(K) Number: K111172 |
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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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4 Series CX phototherapy units equipped with Daavlin's ClearLink Control System software versions v3... | 2 | 05/12/2022 | Daavlin Distributing Company |
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