FDA 510(k) Applications Submitted by LUCID KOREA CO., LTD

FDA 510(k) Number Submission Date Device Name Applicant
K021752 05/28/2002 FP(HEXAFOCON A)RGP CONTACT LENS SPHERICAL/ASP(HEXAFOCON A)RGP CONTACT LENS ASPHERICAL LUCID KOREA CO., LTD


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