510(k) K231613 ยท OHT Light Based Over-The-Counter Hair Removal
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.
| Applicant | Zhuzhou Goldenhot Medical Technology Co., Ltd., Zhuzhou, CN |
| Decision | Substantially Equivalent, Jul 31, 2023 |
| Received | Jun 2, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K231613
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.