ClearanceBrief
510(k) K790251 ยท HQG Lens, Spectacle, Non-Custom (Prescription)

FUL-VUE ASPHERIC CATARACT LENS

ApplicantAmerican Optical Corp., Mchenry IL, US
DecisionSubstantially Equivalent, Feb 26, 1979
ReceivedFeb 6, 1979
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K790251

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.