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FDA 510(k) Applications Submitted by David J Kiefer
FDA 510(k) Number
Submission Date
Device Name
Applicant
K091260
04/29/2009
SERAQUEST EBV EA-D IGG TEST
QUEST INTL., INC.
K152353
08/20/2015
SeraQuest HSV Type 2 Specific IgG
Quest International, Inc.
K162276
08/12/2016
SeraQuest Herpes Type 1 Specific IgG
QUEST INTERNATIONAL, INC
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