FDA 510(k) Applications Submitted by HIROHISA UCHII

FDA 510(k) Number Submission Date Device Name Applicant
K911439 04/02/1991 NON-MYDRIATIC RETINAL CAMERA, CR-45UAF CANON U.S.A., INC.
K895474 09/11/1989 NON-MYDRIATIC RETINAL CAMERA, CR4-45NM DUAL CANON U.S.A., INC.
K895475 09/11/1989 CANON AUTO REF-KERATOMETER RK-2 CANON U.S.A., INC.


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