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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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