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. Device class: 2.
Clearance details
- Applicant
- Varex Imaging Corporation
- Product code
- Code JAA
- Device class
- Class 2
- Regulation
- 21 CFR 892.1650
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Salt Lake City, UT, US
Recent devices under product code JAA
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view all- K193238 — Nexus DR Digital X-Ray Imaging System (with vSharp)
- K190146 — Nexus DR Digital X-ray Imaging System
- K183212 — Nexus DR Digital X-ray Imaging System with stitching
- K181526 — XRpad2 4343 HWC-M Flat Panel Detector
- K172951 — Nexus DR Digital X-ray Imaging System (with PaxScan 4343RC and PaxScan 4343Rv3)
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.