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Soliton, Inc.

FDA 510(k) & PMA Approved Devices — 5 products

Total Devices5
Categories1
Latest FDA decision2021-11-05
TypeNumberDevice NameCodeDateActions
510(k) K212502 Resonic Rapid Acoustic Pulse DeviceGEX2021-11-05 View
510(k) K210964 Resonic Rapid Acoustic Pulse DeviceGEX2021-04-27 View
510(k) K201801 Rapid Acoustic Pulse DeviceGEX2021-01-29 View
510(k) K200331 Rapid Acoustic Pulse DeviceGEX2020-03-10 View
510(k) K190542 Soliton Acoustic Wave DeviceGEX2019-05-24 View
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