510(k) K133019 ยท HQF Laser, Ophthalmic
FIBERION OPHTHALMIC ENDOLASER PROBE
| Applicant | Emtron Elektronik VE Mekanik Sanayi VE Ticaret Lim, Istanbul, TR |
| Decision | Substantially Equivalent, Feb 20, 2015 |
| Received | Sep 26, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K133019
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.