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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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