Architect 1E11-20
Architect 1E11-20 (01E1120) is a Class II device made by Abbott Laboratories, cleared under FDA 510(k) K060709 on 15 Jun 2006 and listed in FDA GUDID since 6 Jun 2016 (UDI-DI 00380740000301), 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 | Number00380740000301 | Date6 Jun 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK060709 | Date15 Jun 2006 | StatusActive |
Official records
- AccessGUDID record 00380740000301
- FDA 510(k) database K060709
Across registries
- FDA 510(k) K060709 decided 15 Jun 2006 Active
- FDA GUDID UDI-DI 00380740000301 listed 6 Jun 2016 Listed
Timeline
- Cleared FDA 510(k) K060709
- Listed FDA GUDID 00380740000301
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Architect
- Generic name
- Gentamicin therapeutic drug monitoring IVD, kit, chemiluminescent immunoassay
- Model / Ref / Catalog
- 1E11-20, 01E1120
- Primary DI / UDI-DI
- 00380740000301
- 510(k) Number
- FDA product code
- LCD
- GMDN term
- Gentamicin therapeutic drug monitoring IVD, kit, chemiluminescent immunoassay
- Device class
- Class II
- Regulation number
- 862.3450
- GUDID distribution status
- In Commercial Distribution
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