FDA 510(k) Applications Submitted by Divya Mavalli

FDA 510(k) Number Submission Date Device Name Applicant
K221889 06/29/2022 ProSomnus EVO [PH] Sleep and Snore Device, ProSomnus EVO [PH] Sleep and Snore Device with Patient Monitoring ProSomnus Sleep Technologies
K202529 09/01/2020 ProSomnus EVO Sleep and Snore Device, ProSomnus EVO Sleep and Snore Device with Patient Monitoring ProSomnus Sleep Technologies, Inc.


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