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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