MEDVOXEL HEARTPRO SOFTWARE APPLICATION— 510(k) K103565

Substantially Equivalent

Medvoxel Systems, Inc.

FDA 510(k) clearance K103565 for MEDVOXEL HEARTPRO SOFTWARE APPLICATION, Substantially Equivalent on 2011-04-12. Applicant: Medvoxel Systems, Inc..

Clearance details

Applicant: Medvoxel Systems, Inc.
Product code: Code LLZ
Advisory panel: Radiology
Date received: 2010-12-06
Decision date: 2011-04-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mississauga, CA

Download summary PDF View on FDA.gov ↗

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.