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FDA 510(k) Applications Submitted by ANGIE BEYER
FDA 510(k) Number
Submission Date
Device Name
Applicant
K131386
05/14/2013
EZ-OX PLUS GENERATION II
AIR LIQUIDE HEALTHCARE AMERICA
K143060
10/24/2014
Intelli-Ox
AIR LIQUIDE HEALTHCARE
K053117
11/07/2005
EZ-OX PLUS
AIR LIQUIDE HEALTHCARE AMERICA
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