ClearanceBrief
510(k) K872855 ยท HJK Lens, Contact, Polymethylmethacrylate, Diagnostic

18MM PEYMAN WIDE FIELD YAG LASER LENS

ApplicantOcular Instruments, Inc., Bellevue WA, US
DecisionSubstantially Equivalent, Sep 4, 1987
ReceivedJul 17, 1987
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K872855

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.