FDA 510(k) Applications Submitted by Leslie Honda

FDA 510(k) Number Submission Date Device Name Applicant
K200331 02/10/2020 Rapid Acoustic Pulse Device Soliton Inc.
K190542 03/04/2019 Soliton Acoustic Wave Device Soliton Inc.
K210964 03/31/2021 Resonic Rapid Acoustic Pulse Device Soliton Inc.
K201801 06/30/2020 Rapid Acoustic Pulse Device Soliton Inc.
K212502 08/09/2021 Resonic Rapid Acoustic Pulse Device Soliton Inc.


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