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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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