Frequencer
510(k) K103176
Frequencer is a medical device (FDA Class II; FDA product code BYI, Percussor, Powered-Electric) made by Dymedso, Inc., cleared under FDA 510(k) K103176 on 26 Jan 2011, active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK103176 | Date26 Jan 2011 | StatusActive |
Official records
- FDA 510(k) database K103176
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- BYI
- Device class
- Class II
- Regulation
- 21 CFR Part 868.5665
- Advisory committee
- Anesthesiology
- FDA decision
- SESE Substantially Equivalent
Devices cleared under K103176
Devices that FDA's GUDID lists as cleared or approved under this submission number. One submission usually covers a whole product family, so the sizes and models are listed here once.
| UDI-DI | Size and differences | |||
|---|---|---|---|---|
| FREQUENCER V2.3 | DYMV2.3 / V2.3 | B401DYMV230 | — | On the market |
| FREQUENCER V2.3 | DYMV2.3 / V2.3 | B402DYMV23 | — | On the market |
| FREQUENCER V2X | DYMV2X / V2X | B401DYMV2X0 | — | On the market |
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