FDA 510(k) Applications Submitted by JAMES HEDGECOCK

FDA 510(k) Number Submission Date Device Name Applicant
K964622 11/18/1996 MEDI-DX 7000 NEURO-DIAGNOSTIC ASSOC.
K980866 02/19/1998 MEDI-DX 7000 CPT WITH AMREX ELECTRODES NEURO-DIAGNOSTIC ASSOC.


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