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OnQ Neuro

K210831 Class II Traditional
Decision Date
2021-11-19
Sponsor / Applicant
Cortechs Labs, Inc.

Technical Specification

510(k) Submission ID K210831
Product Code QIH
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.2050
Decision Date 2021-11-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OnQ Neuro received FDA 510(k) clearance under submission number K210831, sponsored by Cortechs Labs, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2021-11-19.

Classification & Regulation

This clearance is catalogued under FDA product code QIH and 21 CFR 892.2050, within the Radiology review panel as a Class II device.