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FDA 510(k) Applications Submitted by NEUROSCAN
FDA 510(k) Number
Submission Date
Device Name
Applicant
K000865
03/17/2000
QUIK-CAP
NEUROSCAN
K023536
10/21/2002
NUAMPS
NEUROSCAN
K023771
11/12/2002
SYNAMPS2
NEUROSCAN
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