CORONIS 5MP HD, MODEL MDMG 5121— 510(k) K091274

Substantially Equivalent

Barco N.V.

FDA 510(k) clearance K091274 for CORONIS 5MP HD, MODEL MDMG 5121, Substantially Equivalent on 2009-07-14. Applicant: Barco N.V..

Clearance details

Applicant: Barco N.V.
Product code: Code LLZ
Advisory panel: Radiology
Date received: 2009-04-30
Decision date: 2009-07-14
Decision: Substantially Equivalent
Clearance type: Special
Location: Kortrijk, BE

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Adverse events under product code LLZ

product code LLZ

Death: 13
Total: 13

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.