NEXUS DRF DIGITAL X-RAY IMAGING SYSTEM (WITH PAXSCAN 4343CB)— 510(k) K130318

Substantially Equivalent

Varian Medical Systems, X-Ray Products-Infimed

FDA 510(k) clearance K130318 for NEXUS DRF DIGITAL X-RAY IMAGING SYSTEM (WITH PAXSCAN 4343CB), Substantially Equivalent on 2013-04-22. Applicant: Varian Medical Systems, X-Ray Products-Infimed.

Clearance details

Applicant
Varian Medical Systems, X-Ray Products-Infimed
Product code
Code JAA
Advisory panel
Radiology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Special
Location
Liverpool, NY, US
Download summary PDFView on FDA.gov ↗

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.