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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K171024
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Brand Name: Olympus ShockPulse-SE Lithotripsy System with Generator Product Name: ShockPulse-SE Lit... 2 03/05/2026 FEI # 2429304
Olympus Corporation of the Americas
Brand Name: ShockPulse-SE Lithotripsy System SPL-SR Product Name: ShockPulse-SE Lithotripsy System ... 2 02/27/2026 FEI # 2429304
Olympus Corporation of the Americas
Brand Name: ShockPulse-SE Lithotripsy System Product Name: ShockPulse-SE Lithotripsy System - Gener... 2 02/27/2026 FEI # 2429304
Olympus Corporation of the Americas
Brand Name: ShockPulse-SE Lithotripsy System SPL-S Product Name: ShockPulse-SE Lithotripsy System -... 2 02/27/2026 FEI # 2429304
Olympus Corporation of the Americas
Brand Name: Lithotriptor, Ultrasonic Product Name: ShockPulse Lithotripsy Transducer Model/Catalog... 2 11/07/2025 FEI # 2429304
Olympus Corporation of the Americas
ShockPulse-SE Lithotripsy Generator Model/Serial: SPL-S 2 08/11/2022 FEI # 2429304
Olympus Corporation of the Americas
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