ClearanceBrief
510(k) K191024 ยท HQC Unit, Phacofragmentation

xPORT Lens Fragmentation System

ApplicantCarl Zeiss Meditec Cataract Technology, Inc., Reno NV, US
DecisionSubstantially Equivalent, Aug 13, 2019
ReceivedApr 18, 2019
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K191024

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.