Medical Device Recalls
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1 result found
510(K) Number: K961771 |
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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 Surgiwand" II Suction and Irrigation Device: Electrosurgical, cutting & coagulation & acces... | 2 | 04/12/2021 | Covidien |
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