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