Sudo Path
510(k) K131568
Sudo Path is a Class II device made by Ld Technology, LLC, cleared under FDA 510(k) K131568 on 28 Jun 2013, 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 | NumberK131568 | Date28 Jun 2013 | StatusActive |
Official records
- FDA 510(k) database K131568
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- GZO
- Device class
- Class II
- Regulation
- 21 CFR Part 882.1540
- Advisory committee
- Neurology
- FDA decision
- SESE Substantially Equivalent
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