FDA 510(k) Applications Submitted by REICHERT OPHTHALMIC INSTRUMENTS, DIV. LEICA, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K000288 01/31/2000 REICHERT CT200 CONTACT TONOMETER REICHERT OPHTHALMIC INSTRUMENTS, DIV. LEICA, INC.
K964290 10/28/1996 EYECHEK REICHERT OPHTHALMIC INSTRUMENTS, DIV. LEICA, INC.


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