ClearanceBrief
510(k) K900732 ยท HQZ Frame, Spectacle

SPECTACLE FRAME

ApplicantSeiko Corp., Mahwah NJ, US
DecisionSubstantially Equivalent, Jun 20, 1990
ReceivedFeb 16, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K900732

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.