FDA 510(k) Applications Submitted by David Walton

FDA 510(k) Number Submission Date Device Name Applicant
K150572 03/06/2015 Respire Pink Series-Herbst-EF Respire Medical Holding
K152292 08/13/2015 Respire Blue Series-EF Respire Medical Holding
K214096 12/28/2021 Respire Clear Respire Medical, LLC


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