ClearanceBrief
510(k) K945123 ยท HQZ Frame, Spectacle

ARISTAR EYEWEAR, ESPRIT EYEWEAR

ApplicantAristar Inc. U.S.A., Morris Plains NJ, US
DecisionSubstantially Equivalent, Nov 22, 1994
ReceivedOct 19, 1994
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K945123

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.