510(k) K122159 ยท GEX Powered Laser Surgical Instrument
DORNIER MEDILAS H30 SOLVO
| Applicant | Dornier Medtech America, Inc., Kennesaw GA, US |
| Decision | Substantially Equivalent, Feb 1, 2013 |
| Received | Jul 20, 2012 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K122159
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.