510(k) K070355 ยท GEX Powered Laser Surgical Instrument
FOTONA FIDELIS III ER:YAG/ND:YAG LASER SYSTEM FAMILY
| Applicant | Fotona D.D., Ljubljana, SI |
| Decision | Substantially Equivalent, Mar 4, 2008 |
| Received | Feb 6, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K070355
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.