ClearanceBrief
510(k) K133562 ยท HQC Unit, Phacofragmentation

CATARHEX 3

ApplicantOertli Instrumente AG, Berneck, CH
DecisionSubstantially Equivalent, Aug 12, 2014
ReceivedNov 20, 2013
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K133562

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.