FDA 510(k) Applications Submitted by CLEMENT CLARKE, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K961512 04/19/1996 PERKINS HAND-HELD APPLANATION TONOMETER CLEMENT CLARKE, INC.
K952713 06/14/1995 MINI WRIGHT LR AFS CLEMENT CLARKE, INC.


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