Btl-699
510(k) K260691
Btl-699 is a Class II device made by BTL Industries, Inc., cleared under FDA 510(k) K260691 on 23 Aug 2026, 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 | NumberK260691 | Date23 Aug 2026 | StatusActive |
Official records
- FDA 510(k) database K260691
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- OBP
- Device class
- Class II
- Regulation
- 21 CFR Part 882.5805
- Advisory committee
- Neurology
- FDA decision
- SESE Substantially Equivalent
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