Medical Device Recalls
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1 result found
510(K) Number: K121659 |
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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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Brand Name Burn Navigator® Model Numbers: Catalog 1120, Burn Navigator® H2 Catalog 1125, Burn Nav... | 2 | 08/21/2019 | Arcos, Inc |
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