510(k) K231385— Rology Teleradiology Platform (v.1.22.1103)

Substantially Equivalent

Rology, Inc.

Clearance details

Applicant: Rology, Inc.
Product code: Code LLZ
Advisory panel: Radiology
Date received: 2023-05-12
Decision date: 2023-09-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bentonville, AR, US

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.