ClearanceBrief
510(k) K132661 ยท GEX Powered Laser Surgical Instrument

LIGHTSCALPEL

ApplicantLightscalpel, LLC, Woodinville WA, US
DecisionSubstantially Equivalent, Jan 2, 2014
ReceivedAug 26, 2013
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K132661

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.