ClearanceBrief
510(k) K882308 ยท HQG Lens, Spectacle, Non-Custom (Prescription)

CR-39 PLASTIC LENSES FOR EYEGLASSES

ApplicantAutomated Lens System, Miami FL, US
DecisionSubstantially Equivalent, Jul 22, 1988
ReceivedJun 3, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K882308

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.