FDA 510(k) Applications Submitted by Liu Xianwu
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K231613 |
06/02/2023 |
Intense pulsed light device, Model(s): DE01A-B, DE01A-G, DE01B-B, DE01B-G, DE01C-B, DE01C-G, DE02A-B, DE02A-G, DE02B-B, DE02B-G, DE02C-B, DE02C-G. |
Zhuzhou Goldenhot Medical Technology Co., Ltd. |
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