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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