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FDA 510(k) Applications Submitted by RICHARD LOTTI
FDA 510(k) Number
Submission Date
Device Name
Applicant
K073265
11/20/2007
APIERON INSIGHT EXHALED NITRIC OXIDE (ENO) SYSTEM
APIERON, INC.
K172892
09/22/2017
Neuro Assessment System NAS-1000
HeadSense Medical Inc.
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