ClearanceBrief
510(k) K160677 ยท GEX Powered Laser Surgical Instrument

MICRORUPTOR 6

ApplicantMeridian AG, Thun, CH
DecisionSubstantially Equivalent, May 19, 2017
ReceivedMar 10, 2016
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K160677

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.