510(k) K240222 ยท GEX Powered Laser Surgical Instrument
Dermalux Tri-Wave MD MKII (1000021); Dermalux Compact MD (1000024)
| Applicant | Aesthetic Technology, Ltd., Warrington, GB |
| Decision | Substantially Equivalent, Jun 4, 2024 |
| Received | Jan 26, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K240222
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.