FDA 510(k) Applications Submitted by PULMONOX MEDICAL, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K023014 09/10/2002 VIANOX DELIVERY SYSTEM, MODEL I PULMONOX MEDICAL, INC.
K033779 12/04/2003 VIANOX DELIVERY SYSTEM, MODEL II PULMONOX MEDICAL, INC.


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