Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K171024 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Brand Name: Lithotriptor, Ultrasonic Product Name: ShockPulse Lithotripsy Transducer Model/Catalog... | 2 | 11/07/2025 | Olympus Corporation of the Americas |
| ShockPulse-SE Lithotripsy Generator Model/Serial: SPL-S | 2 | 08/11/2022 | Olympus Corporation of the Americas |
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