ClearanceBrief
510(k) K942513 ยท HQZ Frame, Spectacle

SEIKO EYEGLASS FRAME

ApplicantSeiko Optical Products of America, Inc., Mahwah NJ, US
DecisionSubstantially Equivalent, Jul 15, 1994
ReceivedMay 26, 1994
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K942513

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.