Medical Device Recalls
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1 result found
510(K) Number: K171024 |
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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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ShockPulse-SE Lithotripsy Generator Model/Serial: SPL-S | 2 | 08/11/2022 | Olympus Corporation of the Americas |
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