Vidas Rub Igg
510(k) K080766
Vidas Rub Igg is a Class II device made by Biomerieux, Inc., cleared under FDA 510(k) K080766 on 23 Dec 2008, 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 | NumberK080766 | Date23 Dec 2008 | StatusActive |
Official records
- FDA 510(k) database K080766
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- LFX
- Device class
- Class II
- Regulation
- 21 CFR Part 866.3510
- Advisory committee
- Microbiology
- FDA decision
- SESE Substantially Equivalent
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