Valleylab E3810NSB
by Covidien LP
Valleylab E3810NSB is a Class II device made by Covidien LP, cleared under FDA 510(k) K152031 on 17 Sep 2015 and listed in FDA GUDID since 24 Oct 2021 (UDI-DI 10884521823297), active as of 23 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number10884521823297 | Date24 Oct 2021 | StatusListed |
| United States | FDA 510(k)SESE | NumberK152031 | Date17 Sep 2015 | StatusActive |
Official records
- AccessGUDID record 10884521823297
- FDA 510(k) database K152031
Across registries
- FDA 510(k) K152031 decided 17 Sep 2015 Active
- FDA GUDID UDI-DI 10884521823297 listed 24 Oct 2021 Listed
Timeline
- Cleared FDA 510(k) K152031
- Listed FDA GUDID 10884521823297
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Valleylab
- Generic name
- Surgical plume evacuation system tube
- Model / reference
- E3810NSB
- Primary DI / UDI-DI
- 10884521823297
- 510(k) Number
- FDA product code
- GEI
- GMDN term
- Surgical plume evacuation system tube
- Device class
- Class II
- Regulation number
- 878.4400
- GUDID distribution status
- In Commercial Distribution
- Size
- Length — 10 Feet
Similar devices in this category
Other devices filed under Surgical plume evacuation system tube.
- ESU Shroud ICM-000-0449 by I.C. Medical, Inc.
- Smoke Evacuator Wand ICM-000-0075 by I.C. Medical, Inc.
- FUMOVAC 57525328 by Conmed Corporation
- SnapEvac SNAPEVAC20 by Conmed Corporation
- Canister CL500 by Shenzhen Lifotronic Technology Co., Ltd.
- 12067M by Karl Storz SE & CO. KG
- 8668M by Karl Storz SE & CO. KG