510(k) K143713 ยท GEX Powered Laser Surgical Instrument
Lustre PRO Light System
| Applicant | Ambicare Health, Ltd., Livingston, GB |
| Decision | Substantially Equivalent, Jan 19, 2016 |
| Received | Dec 29, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K143713
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.