510(k) K021724 ยท GEX Powered Laser Surgical Instrument
DORNIER DIODE LASER FAMILY, INCLUDING MEDILAS D FIBERTOM, MEDILAS D SKINPULSE & MEDILAS D SKINPULSE S LASER SYSTEMS
| Applicant | Dornier Medtech America, Inc., Kennesaw GA, US |
| Decision | Substantially Equivalent, Aug 19, 2002 |
| Received | May 24, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K021724
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.