pNeuton 58051
pNeuton 58051 is a Class II device made by Airon Corporation, cleared under FDA 510(k) K024344 on 3 Jun 2003 and listed in FDA GUDID since 24 Sep 2016 (UDI-DI 00853678006092), active as of 22 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 | Number00853678006092 | Date24 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK024344 | Date3 Jun 2003 | StatusActive |
Official records
- AccessGUDID record 00853678006092
- FDA 510(k) database K024344
Across registries
- FDA 510(k) K024344 decided 3 Jun 2003 Active
- FDA GUDID UDI-DI 00853678006092 listed 24 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K024344
- Listed FDA GUDID 00853678006092
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- pNeuton
- Generic name
- Anaesthesia breathing circuit, single-use
- Model / Ref / Catalog
- 58051
- Primary DI / UDI-DI
- 00853678006092
- 510(k) Number
- FDA product code
- CBK
- GMDN term
- Anaesthesia breathing circuit, single-use
- Device class
- Class II
- Regulation number
- 868.5895
- GUDID distribution status
- In Commercial Distribution
- Size
- Width — .86 InchLength — .86 InchHeight — 96 InchWeight — .40 Pound
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