ClearanceBrief
510(k) K021752 ยท HQD Lens, Contact (Other Material) - Daily

FP(HEXAFOCON A)RGP CONTACT LENS SPHERICAL/ASP(HEXAFOCON A)RGP CONTACT LENS ASPHERICAL

ApplicantLucid Korea Co., Ltd., Kyungsangbuk-Province, KR
DecisionSubstantially Equivalent, Oct 11, 2002
ReceivedMay 28, 2002
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K021752

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.