FDA 510(k) Applications for Medical Device Product Code "FOA"
(Board, Cardiopulmonary)

FDA 510(k) Number Applicant Device Name Decision Date
K221901 AdvancedCPR Solutions LLC EleGARD 07/29/2022
K191689 Minnesota Resuscitation Solutions, d.b.d AdvancedCPR Solutio EleGARD Patient Positioning System 02/13/2020


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