FDA 510(k) Applications Submitted by Shenzhen Wikkon Precision Technologies Co., Ltd.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K242922 | 09/24/2024 | Extracorporeal Shock Wave Lithotripter (U200) | Shenzhen Wikkon Precision Technologies Co., Ltd. |
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