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FDA 510(k) Applications Submitted by JASON C REYNOLDS
FDA 510(k) Number
Submission Date
Device Name
Applicant
K080294
02/04/2008
ASTORIA-PACIFIC SPOTCHECK BIOTINIDASE MICROPLATE REAGENT KIT
ASTORIA-PACIFIC,INC.
K101392
05/18/2010
NEOPAC SOFTWARE, 3007 DIGITAL PHOTOMETER/FLUOROMETER MODEL NA, 307 AND 350D
ASTORIA-PACIFIC,INC.
K102643
09/14/2010
SPOTCHECK NEONATAL GALT MICROPLATE REAGENT KIT
ASTORIA-PACIFIC,INC.
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