ClearanceBrief
510(k) K180839 ยท HKY Tonometer, Manual

AT 030

ApplicantCarl Zeiss Meditec, AG, Jena, DE
DecisionSubstantially Equivalent, Jun 7, 2018
ReceivedMar 30, 2018
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K180839

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.