SYNERAD OMNI, DIGITAL X-RAY SYSTEM, MODEL AN6250— 510(k) K043025

Substantially Equivalent

Analogic Corp.

FDA 510(k) clearance K043025 for SYNERAD OMNI, DIGITAL X-RAY SYSTEM, MODEL AN6250, Substantially Equivalent on 2004-11-19. Applicant: Analogic Corp..

Clearance details

Applicant: Analogic Corp.
Product code: Code KPR
Advisory panel: Radiology
Date received: 2004-11-03
Decision date: 2004-11-19
Decision: Substantially Equivalent
Clearance type: Abbreviated
Location: Peabody, MA, US

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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.