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Soliton, Inc.

5 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
Resonic Rapid Acoustic Pulse Device (K212502)Soliton, Inc.2021-11-05
Resonic Rapid Acoustic Pulse Device (K210964)Soliton, Inc.2021-04-27
Rapid Acoustic Pulse Device (K201801)Soliton, Inc.2021-01-29
Rapid Acoustic Pulse Device (K200331)Soliton, Inc.2020-03-10
Soliton Acoustic Wave Device (K190542)Soliton, Inc.2019-05-24

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Every clearance here is in the API, with alerts when new ones post.