Medical Device Recalls
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1 result found
510(K) Number: K133348 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Tripolar Hooked Stimulation Probes, L=20mm, Reference Number SI3H0020S2526D. Used during intraopera... | 2 | 06/25/2021 | Spes Medica |
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