Avanos 42839
Avanos 42839 (8140-24-2.3) is a Class II device made by Avanos Medical, Inc., cleared under FDA 510(k) K043114 on 10 Dec 2004 and listed in FDA GUDID since 20 Feb 2019 (UDI-DI 00350770428390), 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 | Number00350770428390 | Date20 Feb 2019 | StatusListed |
| United States | FDA 510(k)SESE | NumberK043114 | Date10 Dec 2004 | StatusActive |
Official records
- AccessGUDID record 00350770428390
- FDA 510(k) database K043114
Across registries
- FDA 510(k) K043114 decided 10 Dec 2004 Active
- FDA GUDID UDI-DI 00350770428390 listed 20 Feb 2019 Listed
Timeline
- Cleared FDA 510(k) K043114
- Listed FDA GUDID 00350770428390
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Avanos
- Generic name
- Gastrostomy button
- Model / Ref / Catalog
- 42839, 8140-24-2.3
- Primary DI / UDI-DI
- 00350770428390
- 510(k) Number
- FDA product code
- KNT
- GMDN term
- Gastrostomy button
- Device class
- Class II
- Regulation number
- 876.5980
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Conditional
- Size
- Catheter Gauge — 24 French