ClearanceBrief
510(k) K943086 ยท HQZ Frame, Spectacle

SPECTACLE FRAME

ApplicantRadiant Spectacles Manufacturers, Baltimore MD, US
DecisionSubstantially Equivalent, Aug 2, 1994
ReceivedJun 28, 1994
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K943086

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.