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FDA 510(k) Applications Submitted by SYNAPSYS, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K012415
07/30/2001
AURIS AEP
SYNAPSYS, INC.
K982103
06/15/1998
ULMER (VNG) VIDEO NYSTAGMOGRAPH
SYNAPSYS, INC.
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