ClearanceBrief
510(k) K123682 ยท GEX Powered Laser Surgical Instrument

INMODE HAIR REMOVAL (HR) DEVICE

ApplicantInmode MD , Ltd., Kfar Saba, IL
DecisionSubstantially Equivalent, Feb 27, 2013
ReceivedNov 30, 2012
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K123682

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.