ViaMed 13312
ViaMed 13312 is a Class II device made by Rece International Corp., cleared under FDA 510(k) K043286 on 13 Jan 2005 and listed in FDA GUDID since 23 May 2017 (UDI-DI 00811382010682), 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 | Number00811382010682 | Date23 May 2017 | StatusListed |
| United States | FDA 510(k)SESE | NumberK043286 | Date13 Jan 2005 | StatusActive |
Official records
- AccessGUDID record 00811382010682
- FDA 510(k) database K043286
Across registries
- FDA 510(k) K043286 decided 13 Jan 2005 Active
- FDA GUDID UDI-DI 00811382010682 listed 23 May 2017 Listed
Timeline
- Cleared FDA 510(k) K043286
- Listed FDA GUDID 00811382010682
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- ViaMed
- Generic name
- Aneroid manual sphygmomanometer
- Model / reference
- 13312
- Primary DI / UDI-DI
- 00811382010682
- 510(k) Number
- FDA product code
- DXQ
- GMDN term
- Aneroid manual sphygmomanometer
- Device class
- Class II
- Regulation number
- 870.1120
- GUDID distribution status
- In Commercial Distribution
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