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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