VISCO 360 Viscosurgical System
510(k) K171905
VISCO 360 Viscosurgical System is a Class II device made by Sight Sciences, Inc., cleared under FDA 510(k) K171905 on 27 Jul 2017, active as of 10 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 | NumberK171905 | Date27 Jul 2017 | StatusActive |
Official records
- FDA 510(k) database K171905
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- MRH
- Device class
- Class II
- Regulation
- 21 CFR Part 880.5725
- Advisory committee
- General Hospital
- FDA decision
- SESE Substantially Equivalent