510(k) K070536 ยท GEX Powered Laser Surgical Instrument
MEDILAS D FAMILY LASERS
| Applicant | Dornier Medtech America, Inc., Kennesaw GA, US |
| Decision | Substantially Equivalent, May 21, 2007 |
| Received | Feb 26, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K070536
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.