FDA 510(k) Applications Submitted by KIM PETERSON

FDA 510(k) Number Submission Date Device Name Applicant
K001179 04/11/2000 SUPER NOVA, ACUBEAM LIGHT FORCE THERAPY, INC.
K042731 10/01/2004 ARCHITECT CA 125 II ASSAY FUJIREBIO DIAGNOSTICS, INC.
K042732 10/01/2004 ARCHITECT CA 15-3 ASSAY FUJIREBIO DIAGNOSTICS, INC.
K033731 11/28/2003 AXSYM CORTISOL ASSAY FUJIREBIO DIAGNOSTICS, INC.


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