Avanos 182122
Avanos 182122 is a Class II device made by Avanos Medical, Inc., cleared under FDA 510(k) K000495 on 28 Mar 2000 and listed in FDA GUDID since 25 Sep 2019 (UDI-DI 00193493933167), 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 | Number00193493933167 | Date25 Sep 2019 | StatusListed |
| United States | FDA 510(k)SESE | NumberK000495 | Date28 Mar 2000 | StatusActive |
Official records
- AccessGUDID record 00193493933167
- FDA 510(k) database K000495
Across registries
- FDA 510(k) K000495 decided 28 Mar 2000 Active
- FDA GUDID UDI-DI 00193493933167 listed 25 Sep 2019 Listed
Timeline
- Cleared FDA 510(k) K000495
- Listed FDA GUDID 00193493933167
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Avanos
- Generic name
- Peripheral anaesthesia catheter set, non-medicated
- Model / Ref / Catalog
- 182122
- Primary DI / UDI-DI
- 00193493933167
- 510(k) Number
- FDA product code
- BSP
- GMDN term
- Peripheral anaesthesia catheter set, non-medicated
- Device class
- Class II
- Regulation number
- 868.5150
- GUDID distribution status
- In Commercial Distribution
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