Medical Device Recalls
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1 result found
510(K) Number: K192265 |
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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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GI4000 Electrosurgical Unit - intended to deliver electrosurgical outputs to perform cutting and/or ... | 2 | 11/16/2022 | Steris Corporation |
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