FDA 510(k) Applications Submitted by Contego Medical Inc.

FDA 510(k) Number Submission Date Device Name Applicant
K221204 04/26/2022 Excipio SV Thrombectomy Device Contego Medical Inc.
K221339 05/09/2022 Paladin Carotid Post-Dilation Balloon System with Integrated Embolic Protection Contego Medical Inc.
K223897 12/28/2022 Excipio LV Thrombectomy Device Contego Medical Inc.


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