ClearanceBrief
510(k) K920571 ยท HPC Set, Lens, Trial, Ophthalmic

TRIAL LENS SET

ApplicantR.H. Burton Co., Grove City OH, US
DecisionSubstantially Equivalent, May 7, 1992
ReceivedFeb 7, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K920571

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.