meddevicedb.com FDA Device Reference

TaiChiC

K203250 Class II Traditional
Decision Date
2021-03-12
Sponsor / Applicant
Our United Corporation

Technical Specification

510(k) Submission ID K203250
Product Code IWB
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.5750
Decision Date 2021-03-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TaiChiC received FDA 510(k) clearance under submission number K203250, sponsored by Our United Corporation. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2021-03-12.

Classification & Regulation

This clearance is catalogued under FDA product code IWB and 21 CFR 892.5750, within the Radiology review panel as a Class II device.