FDA 510(k) Applications Submitted by ALAN NICHOL

FDA 510(k) Number Submission Date Device Name Applicant
K984343 12/04/1998 PREMIER TYPE SPECIFIC HSV-1 IGG ELISA TEST MERIDIAN DIAGNOSTICS, INC.
K984346 12/04/1998 PREMIER TYPE SPECIFIC HSV-2 IGG ELISA TEST MERIDIAN DIAGNOSTICS, INC.


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