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FDA 510(k) Applications Submitted by CLASS A ENT.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K982053
06/11/1998
EEG ELECTRODES MODEL 445 SERIES
CLASS A ENT.
K021118
04/08/2002
DETACHABLE MONOPOLAR EMG NEEDLE, MODELS 610-725, 610-737, 610-637, 610-744, 610-650, 610-570
CLASS A ENT.
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