Thyretain 40-540050.V2
Thyretain 40-540050.V2 is a Class II device made by Diagnostic Hybrids, Inc., cleared under FDA 510(k) K092229 on 18 May 2010 and listed in FDA GUDID since 7 Aug 2018 (UDI-DI 30014613331636), 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 | Number30014613331636 | Date7 Aug 2018 | StatusListed |
| United States | FDA 510(k)SESE | NumberK092229 | Date18 May 2010 | StatusActive |
Official records
- AccessGUDID record 30014613331636
- FDA 510(k) database K092229
Across registries
- FDA 510(k) K092229 decided 18 May 2010 Active
- FDA GUDID UDI-DI 30014613331636 listed 7 Aug 2018 Listed
Timeline
- Cleared FDA 510(k) K092229
- Listed FDA GUDID 30014613331636
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Thyretain
- Generic name
- Thyroid stimulating hormone receptor (TSHR) antibody IVD, kit, bioassay
- Model / Ref / Catalog
- 40-540050.V2
- Primary DI / UDI-DI
- 30014613331636
- 510(k) Number
- FDA product code
- JZO
- GMDN term
- Thyroid stimulating hormone receptor (TSHR) antibody IVD, kit, bioassay
- Device class
- Class II
- Regulation number
- 866.5870
- GUDID distribution status
- In Commercial Distribution
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