ClearanceBrief
510(k) K170667 ยท GWG Endoscope, Neurological

QEVO System with KINEVO 900

ApplicantCarl Zeiss Meditec, AG, Jena, DE
DecisionSubstantially Equivalent, Aug 18, 2017
ReceivedMar 6, 2017
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K170667

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.