Viva Eb
by Etview, Ltd.
510(k) K120334
Viva Eb is a Class II device made by Etview, Ltd., cleared under FDA 510(k) K120334 on 8 Jun 2012, 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 | NumberK120334 | Date8 Jun 2012 | StatusActive |
Official records
- FDA 510(k) database K120334
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- CBI
- FDA applicant
- Etview , Ltd.
- Device class
- Class II
- Regulation
- 21 CFR Part 868.5740
- Advisory committee
- Anesthesiology
- FDA decision
- SESE Substantially Equivalent
Devices cleared under K120334
Devices that FDA's GUDID lists as cleared or approved under this submission number. One submission usually covers a whole product family, so the sizes and models are listed here once.
| UDI-DI | Size and differences | |||
|---|---|---|---|---|
| VivaSight AS Pack Set include TVEB70100AS | TVEB70100AS / TVEB70100AS | 07290013745774 | — | On the market |
| VivaSight AS Pack Set include TVEB75105AS | TVEB75105AS / TVEB75105AS | 07290013745781 | — | On the market |
| VivaSight AS Pack Set include TVEB80110AS | TVEB80110AS / TVEB80110AS | 07290013745798 | — | On the market |
| VivaSight Pack TVEB70100 | TVEB70100 / TVEB70100 | 07290013745545 | — | On the market |
| VivaSight Pack TVEB75105 | TVEB75105 / TVEB75105 | 07290013745552 | — | On the market |
| VivaSight Pack TVEB80110 | TVEB80110 / TVEB80110 | 07290013745569 | Length 8 mm | On the market |
| VivaSight-EB EBB09700 | EBB09700 / EBB09700 | 07290013745514 | — | On the market |
| VivaSight-EB EBB09700AS | EBB09700AS / EBB09700AS | 07290013745804 | — | On the market |
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Other devices filed under FDA product code CBI (Tube, Tracheal/Bronchial, Differential Ventilation (W/Wo Connector)).
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