ClearanceBrief
510(k) K020071 ยท GEX Powered Laser Surgical Instrument

VIRIDIS DERMA LASER

ApplicantQuantel Medical, Hot Springs AR, US
DecisionSubstantially Equivalent, Apr 5, 2002
ReceivedJan 9, 2002
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K020071

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.