510(k) K083899 ยท GEX Powered Laser Surgical Instrument
REVLITE Q-SWITCHED ND:YAG LASER SYSTEM
| Applicant | Hoya Conbio, Inc., Twain Harte CA, US |
| Decision | Substantially Equivalent, Jun 1, 2009 |
| Received | Dec 29, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K083899
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.