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FDA 510(k) Applications Submitted by CHARLES A PETERSON
FDA 510(k) Number
Submission Date
Device Name
Applicant
K090940
04/03/2009
SPOTCHECK BLOOD SPOT CONTROL, ASSAYED
ASTORIA-PACIFIC,INC.
K121101
04/11/2012
SPOTCHECK NEONATAL TOTAL GALACTOSE MICROPLATE REAGENT KIT
ASTORIA-PACIFIC,INC.
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