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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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