meddevicedb.com FDA Device Reference

Real Intelligence Cori

K193120 Class II Traditional
Decision Date
2020-02-14
Sponsor / Applicant
Blue Belt Technologies, Inc.

Technical Specification

510(k) Submission ID K193120
Product Code OLO
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.4560
Decision Date 2020-02-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Real Intelligence Cori received FDA 510(k) clearance under submission number K193120, sponsored by Blue Belt Technologies, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2020-02-14.

Classification & Regulation

This clearance is catalogued under FDA product code OLO and 21 CFR 882.4560, within the Neurology review panel as a Class II device.