Medical Device Recalls
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1 result found
510(K) Number: K033003 |
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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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| Foot Controlled Electrosurgical Suction Coagulator, Electrosurgical Suction Coagulator 10FR, Catalog... | 2 | 12/09/2022 |
FEI # 3001451571 ConMed Corporation |
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