EOS System— 510(k) K142773

Substantially Equivalent

Eos Imaging

FDA 510(k) clearance K142773 for EOS System, Substantially Equivalent on 2015-01-22. Applicant: Eos Imaging.

Clearance details

Applicant: Eos Imaging
Product code: Code KPR
Advisory panel: Radiology
Date received: 2014-09-25
Decision date: 2015-01-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Paris, FR

Download summary PDF View on FDA.gov ↗

Adverse events under product code KPR

product code KPR

Other: 6
Total: 6

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.