Qb Test
by Qbtech AB
510(k) K133382
Qb Test is a device classified as Unclassified made by Qbtech AB, cleared under FDA 510(k) K133382 on 24 Mar 2014, active as of 12 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 | NumberK133382 | Date24 Mar 2014 | StatusActive |
Official records
- FDA 510(k) database K133382
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- LQD
- Device class
- U
- Advisory committee
- Unknown
- FDA decision
- SESE Substantially Equivalent
Devices cleared under K133382
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 | |||
|---|---|---|---|---|
| QbTest | QbTest | 07350103930067 | — | On the market |
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