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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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