Nexus DRF Digital X-ray Imaging System— 510(k) K253103
Substantially EquivalentVarex Imaging Corporation
FDA 510(k) clearance K253103 for Nexus DRF Digital X-ray Imaging System, Substantially Equivalent on 2026-05-29. Applicant: Varex Imaging Corporation.
Clearance details
- Applicant
- Varex Imaging Corporation
- Product code
- Code JAA
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Salt Lake City, UT, US
Adverse events under product code JAA
product code JAA- Other
- 1
- Total
- 1
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.