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FDA 510(k) Applications Submitted by PULMONE ADVANCED MEDICAL DEVICES, LTD
FDA 510(k) Number
Submission Date
Device Name
Applicant
K161295
05/09/2016
MiniBox +
PULMONE ADVANCED MEDICAL DEVICES, LTD
K133051
09/27/2013
PULMONE MINIBOX PFT TM
PULMONE ADVANCED MEDICAL DEVICES, LTD
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