Medical Device Recalls
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1 result found
510(K) Number: K153389 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| inLight Medical LED Pads used with Polychromatic light technology system | 3 | 06/24/2021 |
FEI # 3010709091 Inlightened Partners LLC |
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