Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K062720 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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CUTTING ELECTRODE BIPO 24.5FR, REF 4653.1323 | 2 | 08/12/2021 | Richard Wolf GmbH |
Individual units labeled in part: REF: 4630022; for S(a)line resectoscopes; Vaporization electrode, ... | 2 | 11/04/2013 | Richard Wolf Medical Instruments Corp. |
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