FDA 510(k) Applications Submitted by Zhuzhou Goldenhot Medical Technology Co., Ltd.
| 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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