AbbVie J AV062
by Abbvie Inc.
AbbVie J AV062 is a Class II device made by Abbvie Inc., cleared under FDA 510(k) K142816 on 14 Jan 2015 and listed in FDA GUDID since 15 Apr 2019 (UDI-DI 08054083014432), 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 | Number08054083014432 | Date15 Apr 2019 | StatusListed |
| United States | FDA 510(k)SESE | NumberK142816 | Date14 Jan 2015 | StatusActive |
Official records
- AccessGUDID record 08054083014432
- FDA 510(k) database K142816
Across registries
- FDA 510(k) K142816 decided 14 Jan 2015 Active
- FDA GUDID UDI-DI 08054083014432 listed 15 Apr 2019 Listed
Timeline
- Cleared FDA 510(k) K142816
- Listed FDA GUDID 08054083014432
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- AbbVie J
- Generic name
- Jejunostomy tube
- Model / reference
- AV062
- Primary DI / UDI-DI
- 08054083014432
- 510(k) Number
- FDA product code
- KNT
- GMDN term
- Jejunostomy tube
- Device class
- Class II
- Regulation number
- 876.5980
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Conditional
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