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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