Medical Device Recalls
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1 result found
510(K) Number: K211269 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Visualase Cooled Laser Applicator System (VCLAS) 9735560 .4MM CORE FIBER 10MM TIP product. Used to... | 2 | 11/17/2022 |
FEI # 1000517638 Medtronic Navigation, Inc. |
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