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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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