meddevicedb.com FDA Device Reference

Neuro.Al Algorithm

K200750 Class II Special
Decision Date
2020-11-06
Sponsor / Applicant
Terarecon,Inc.

Technical Specification

510(k) Submission ID K200750
Product Code LLZ
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.2050
Decision Date 2020-11-06
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Neuro.Al Algorithm received FDA 510(k) clearance under submission number K200750, sponsored by Terarecon,Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2020-11-06.

Classification & Regulation

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