Frequencer Model V2X
510(k) K100749
Frequencer Model V2X is a medical device (FDA Class II; FDA product code BYI, Percussor, Powered-Electric) made by Dymedso, Inc., cleared under FDA 510(k) K100749 on 31 Aug 2010, 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 | NumberK100749 | Date31 Aug 2010 | StatusActive |
Official records
- FDA 510(k) database K100749
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- Withdrawn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
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