VivaSight-SL (TVT) system
by Etview, Ltd.
510(k) K181880
VivaSight-SL (TVT) system is a Class II device made by Etview, Ltd., cleared under FDA 510(k) K181880 on 29 Nov 2018, 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 | NumberK181880 | Date29 Nov 2018 | StatusActive |
Official records
- FDA 510(k) database K181880
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- BTR
- FDA applicant
- Etview , Ltd.
- Device class
- Class II
- Regulation
- 21 CFR Part 868.5730
- Advisory committee
- Anesthesiology
- FDA decision
- SESE Substantially Equivalent
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