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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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