Sentinel Uibc Liquid
510(k) K051111
Sentinel Uibc Liquid is a Class I device made by Sentinel Ch. Srl, cleared under FDA 510(k) K051111 on 17 Nov 2005, active as of 11 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 | NumberK051111 | Date17 Nov 2005 | StatusActive |
Official records
- FDA 510(k) database K051111
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- JQF
- Device class
- Class I
- Regulation
- 21 CFR Part 862.1415
- Advisory committee
- Clinical Chemistry
- FDA decision
- SESE Substantially Equivalent
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