NEXUS DRF DIGITAL X-RAY IMAGING SYSTEM— 510(k) K103416

Substantially Equivalent

Infimed, Inc.

FDA 510(k) clearance K103416 for NEXUS DRF DIGITAL X-RAY IMAGING SYSTEM, Substantially Equivalent on 2011-03-17. Applicant: Infimed, Inc..

Clearance details

Applicant: Infimed, Inc.
Product code: Code OWB
Advisory panel: Radiology
Date received: 2010-11-22
Decision date: 2011-03-17
Decision: Substantially Equivalent
Clearance type: Special
Location: Great Neck, NY, US

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Adverse events under product code OWB

product code OWB

Death: 49
Injury: 340
Malfunction: 36,973
Total: 37,362

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. 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.