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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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