TRAQinform IQ— 510(k) K233998

Substantially Equivalent

Aiq Global, Inc.

FDA 510(k) clearance K233998 for TRAQinform IQ, Substantially Equivalent on 2024-09-05. Applicant: Aiq Global, Inc..

Clearance details

Applicant: Aiq Global, Inc.
Product code: Code LLZ
Advisory panel: Radiology
Date received: 2023-12-18
Decision date: 2024-09-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Madison, WI, 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.