VIDAR VISION 3000 AND 4000 X-RAY SYSTEMS
FDA 510(k) clearance K071193 · decided 2007-05-30
Clearance details
- K-number
- K071193
- Device name
- VIDAR VISION 3000 AND 4000 X-RAY SYSTEMS
- Applicant
- Vidar Systems Corp.
- Decision
- Substantially Equivalent
- Date received
- 2007-04-30
- Decision date
- 2007-05-30
- Days to decision
- 30 days
- Clearance type
- Special
- Product code
- MQB
- Device class
- 2
- Regulation number
- 892.1680
- Medical specialty
- Radiology
- Advisory committee
- Radiology
- Location
- Deer Field, IL, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.