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FDA 510(k) Applications Submitted by AEIOMED, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K100121
01/15/2010
MODEL 300157 CPAP SYSTEM
AEIOMED, INC.
K072993
10/23/2007
REUSABLE HEADREST WITH NASAL SEAL
AEIOMED, INC.
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