Tumor Marker Control level 2 91302
Tumor Marker Control level 2 91302 is a Class I device made by Cliniqa Corporation, cleared under FDA 510(k) K030705 on 26 Mar 2003 and listed in FDA GUDID since 22 Aug 2018 (UDI-DI 00817238010127), active as of 8 Nov 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 | Number00817238010127 | Date22 Aug 2018 | StatusListed |
| United States | FDA 510(k)SESE | NumberK030705 | Date26 Mar 2003 | StatusActive |
Official records
- AccessGUDID record 00817238010127
- FDA 510(k) database K030705
Across registries
- FDA 510(k) K030705 decided 26 Mar 2003 Active
- FDA GUDID UDI-DI 00817238010127 listed 22 Aug 2018 Listed
Timeline
- Cleared FDA 510(k) K030705
- Listed FDA GUDID 00817238010127
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Tumor Marker Control level 2
- Generic name
- Multiple-type clinical chemistry analyte profile IVD, control
- Model / reference
- 91302
- Primary DI / UDI-DI
- 00817238010127
- 510(k) Number
- FDA product code
- JJY
- GMDN term
- Multiple-type clinical chemistry analyte profile IVD, control
- Device class
- Class I
- Regulation number
- 862.1660
- GUDID distribution status
- In Commercial Distribution
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