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FDA 510(k) Applications Submitted by VIVOSONIC, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K080060
01/09/2008
VIVOSONIC NEUROSCREEN
VIVOSONIC, INC.
K043396
12/10/2004
INTEGRITY, MODEL V500
VIVOSONIC, INC.
K003364
10/27/2000
VIVO 200 DPS VIVOSCAN
VIVOSONIC, INC.
K033108
09/30/2003
VIVO 200 DPS VIVOSCAN VERSION 2.0 OAE AUDIOMETER
VIVOSONIC, INC.
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