510(k) K080959 ยท GEX Powered Laser Surgical Instrument
DORNIER MEDILAS D 30 LASER, MEDILAS D 1064
| Applicant | Dornier Medtech America, Inc., Kennesaw GA, US |
| Decision | Substantially Equivalent, Jun 27, 2008 |
| Received | Apr 3, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K080959
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.