Product areas
FDA product code distribution
Soliton, Inc.
Country / region:United States (US)
510(k) submissions
5
Filtered: GEX
Latest clearance
2021-11-05
Product codes
1
GEX
510(k) submissions
5 total · filtered by GEX
| K number | Device name | Product code | Class | Decision date |
|---|---|---|---|---|
| K212502 | Resonic Rapid Acoustic Pulse Device | GEX | Class 2 | 2021-11-05 |
| K210964 | Resonic Rapid Acoustic Pulse Device | GEX | Class 2 | 2021-04-27 |
| K201801 | Rapid Acoustic Pulse Device | GEX | Class 2 | 2021-01-29 |
| K200331 | Rapid Acoustic Pulse Device | GEX | Class 2 | 2020-03-10 |
| K190542 | Soliton Acoustic Wave Device | GEX | Class 2 | 2019-05-24 |
Company profile
- Canonical name
- Soliton, Inc.
- Country
- United States(US)
Cited predicates
7Cited as predicate
7- K222629
Resonic Rapid Acoustic Pulse Device
- K222629
Resonic Rapid Acoustic Pulse Device
- K212502
Resonic Rapid Acoustic Pulse Device
- K212502
Resonic Rapid Acoustic Pulse Device
- K210964
Resonic Rapid Acoustic Pulse Device
- K201801
Rapid Acoustic Pulse Device
- K200331
Rapid Acoustic Pulse Device
7 submissions cite Soliton, Inc. as a predicate