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FDA 510(k) Applications Submitted by DIOPSYS INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K043491
12/17/2004
ENFANTTM
DIOPSYS INC.
K101763
06/23/2010
DIOPSYS NOVA VEP VISION TESTING SYSTEM
DIOPSYS INC.
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