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FDA 510(k) Applications Submitted by APIERON, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K083617
12/08/2008
APIERON INSIGHT ENO SYSTEM
APIERON, INC.
K073265
11/20/2007
APIERON INSIGHT EXHALED NITRIC OXIDE (ENO) SYSTEM
APIERON, INC.
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