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OPAL CHIRO, 20/20 P-DR

K141435 Class II Traditional
Decision Date
2014-08-27
Sponsor / Applicant
2020 Imaging

Technical Specification

510(k) Submission ID K141435
Product Code MQB
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1680
Decision Date 2014-08-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OPAL CHIRO, 20/20 P-DR received FDA 510(k) clearance under submission number K141435, sponsored by 2020 Imaging. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2014-08-27.

Classification & Regulation

This clearance is catalogued under FDA product code MQB and 21 CFR 892.1680, within the Radiology review panel as a Class II device.