FDA 510(k) Applications Submitted by BIODEX MEDICAL SYSTEMS, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K090296 02/06/2009 ATOMLAB 400 AND ATOMLAB 500 DOSE CALIBRATORS, MODELS 086-330, -331, -332, -335 AND -336 BIODEX MEDICAL SYSTEMS, INC.
K063666 12/11/2006 SHARPS CONTAINER, MODEL 039-413 BIODEX MEDICAL SYSTEMS, INC.


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