ClearanceBrief
510(k) K123443 ยท GEX Powered Laser Surgical Instrument

PRECISE SHP DIODE LASER

ApplicantCAO Group, Inc., West Jordan UT, US
DecisionSubstantially Equivalent, Aug 13, 2013
ReceivedNov 8, 2012
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K123443

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.