Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

TRAQinform IQ

K-Number: K233998 · 2024-09-05

ApplicantAiq Global, Inc.
Decision Date2024-09-05
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

TRAQinform IQ is a medical device manufactured by Aiq Global, Inc.. It received FDA 510(k) clearance on 2024-09-05 under approval number K233998. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRAQinform IQ?

TRAQinform IQ is a medical device that received FDA 510(k) clearance on 2024-09-05. It is manufactured by Aiq Global, Inc.. The 510(k) number is K233998.

When was TRAQinform IQ approved by the FDA?

TRAQinform IQ received FDA 510(k) clearance on 2024-09-05, under approval number K233998.

What company makes TRAQinform IQ?

TRAQinform IQ is manufactured by Aiq Global, Inc..

What is the FDA product code for TRAQinform IQ?

The FDA product code for TRAQinform IQ is LLZ.

Related Devices (Code: LLZ)

K161959ClearView cCADClearview Diagnostics, Inc. K163539Ez3D-i / E3Ewoosoft Co., Ltd. K162955Multi-Modality Tumor Tracking (MMTT) applicationPhilips Medical Systems Nederland B.V. K160852ZiaZetta Medical Technologies, LLC K162376CAAS MR 4D FlowPie Medical Imaging BV K161322CT CoPilotZepmed, LLC

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑