510(k) K123385 ยท GEX Powered Laser Surgical Instrument
MEDILAS H LASER FIBERS
| Applicant | Dornier Medtech America, Inc., Kennesaw GA, US |
| Decision | Substantially Equivalent, Dec 14, 2012 |
| Received | Nov 2, 2012 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K123385
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.