meddevicedb.com FDA Device Reference

UB ERP System

K253767 Class II Traditional
Decision Date
2026-06-30
Sponsor / Applicant
Universal Brain

Technical Specification

510(k) Submission ID K253767
Product Code OLT
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.1400
Decision Date 2026-06-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

UB ERP System received FDA 510(k) clearance under submission number K253767, sponsored by Universal Brain. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2026-06-30.

Classification & Regulation

This clearance is catalogued under FDA product code OLT and 21 CFR 882.1400, within the Neurology review panel as a Class II device.