ClearanceBrief
510(k) K151575 ยท LXQ Cup, Eye

Dynarex Eye Cups

ApplicantDynarex Corporation, Orangeburg NY, US
DecisionSubstantially Equivalent, Sep 1, 2015
ReceivedJun 11, 2015
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K151575

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.