Medical Device Recalls
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1 result found
510(K) Number: K191601 |
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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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Covidien Valleylab FT10, FT Series Energy Platform, REF: VLFT10GEN, DLVLFT10GEN, VLFT10GENZD | 2 | 01/03/2024 | Covidien |
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