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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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