Vidar Vision 2000
510(k) K070563
Vidar Vision 2000 is a Class II device made by Vidar Systems Corp., cleared under FDA 510(k) K070563 on 16 Mar 2007, 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 | FDA 510(k)SESE | NumberK070563 | Date16 Mar 2007 | StatusActive |
Official records
- FDA 510(k) database K070563
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- MQB
- Device class
- Class II
- Regulation
- 21 CFR Part 892.1680
- Advisory committee
- Radiology
- FDA decision
- SESE Substantially Equivalent
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