FDA 510(k) Applications Submitted by COPD PARTNERS, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K071461 05/25/2007 MODEL 300D HOME OXYGEN LIQUEFIER COPD PARTNERS, INC.
K072011 07/23/2007 COPD LIQUID OXYGEN PORTABLE, MODEL 300P COPD PARTNERS, INC.


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