510(k) K120810 ยท GEX Powered Laser Surgical Instrument
FIBEROPTIC LASER DELIVERY SYSTEM
| Applicant | Fiberoptic Fabrications, Inc., Wilbraham MA, US |
| Decision | Substantially Equivalent, Jun 28, 2012 |
| Received | Mar 16, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K120810
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.