FDA 510(k) Applications Submitted by JASON 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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