ClearanceBrief
510(k) K123293 ยท GEX Powered Laser Surgical Instrument

PASTELLE Q-SWITCHED ND: YAG LASER

ApplicantWon Technology Co., Ltd., Woodinville WA, US
DecisionSubstantially Equivalent, Apr 11, 2013
ReceivedOct 22, 2012
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K123293

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.