ProVia 3 3PROV180HS
ProVia 3 3PROV180HS is a Class II device made by Medtronic, Inc., cleared under FDA 510(k) K140695 on 12 Jun 2014 and listed in FDA GUDID since 6 Feb 2022 (UDI-DI 00763000569914), 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 | Number00763000569914 | Date6 Feb 2022 | StatusListed |
| United States | FDA 510(k)SESE | NumberK140695 | Date12 Jun 2014 | StatusActive |
Official records
- AccessGUDID record 00763000569914
- FDA 510(k) database K140695
Across registries
- FDA 510(k) K140695 decided 12 Jun 2014 Active
- FDA GUDID UDI-DI 00763000569914 listed 6 Feb 2022 Listed
Timeline
- Cleared FDA 510(k) K140695
- Listed FDA GUDID 00763000569914
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- ProVia 3
- Generic name
- Cardiac/peripheral vascular guidewire, single-use
- Model / reference
- 3PROV180HS
- Primary DI / UDI-DI
- 00763000569914
- 510(k) Number
- FDA product code
- DQX
- GMDN term
- Cardiac/peripheral vascular guidewire, single-use
- Device class
- Class II
- Regulation number
- 870.1330
- GUDID distribution status
- In Commercial Distribution
- Size
- Outer Diameter — 0.014 InchLength — 180.0 Centimeter
Similar devices in this category
Other devices filed under Cardiac/peripheral vascular guidewire, single-use.