ClearanceBrief
510(k) K171506 ยท EWO Audiometer

Easyscreen

ApplicantMaico Diagnostics GmbH, Berlin, DE
DecisionSubstantially Equivalent, Aug 29, 2017
ReceivedMay 23, 2017
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K171506

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.