FDA 510(k) Applications for Medical Device Product Code "SDT"

FDA 510(k) Number Applicant Device Name Decision Date
K241091 Inogen, Inc. SIMEOX 200 Airway Clearance Device 12/23/2024
K122111 RESPIRONICS, INC. RESPIRONICS SIMPLYCLEAR DEVICE 12/31/2012
K133057 Westmed, Inc. VIBRALUNG ACOUSTICAL PERCUSSOR 05/23/2014


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