ClearanceBrief
510(k) K800192 ยท HPX Lens, Contact (Polymethylmethacrylate)

DURALITE LENS

ApplicantAmerican Optical Corp., Mchenry IL, US
DecisionSubstantially Equivalent, Mar 12, 1980
ReceivedJan 29, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K800192

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.