Class Class II

Extracorporeal Shock Wave Lithotripter (U200) (K242922)

K242922 2025-06-18 Traditional
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Description

Extracorporeal Shock Wave Lithotripter (U200) by Shenzhen Wikkon Precision Technologies Co., Ltd., an FDA 510(k) cleared gastroenterology, urology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK242922
Clearance Date2025-06-18
Clearance TypeTraditional
Product CodeLNS
Regulation Number876.5990

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