ULTRAPACS— 510(k) K051813

Substantially Equivalent

Ultrarad Corporation

FDA 510(k) clearance K051813 for ULTRAPACS, Substantially Equivalent on 2005-08-15. Applicant: Ultrarad Corporation.

Clearance details

Applicant: Ultrarad Corporation
Product code: Code LLZ
Advisory panel: Radiology
Date received: 2005-07-05
Decision date: 2005-08-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Denton, TX, US

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.