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JOINT MOTON IMAGER(TM)

K902583 Class II Traditional
Decision Date
1990-09-27
Sponsor / Applicant
Concord Imaging, Ltd.

Technical Specification

510(k) Submission ID K902583
Product Code JAA
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1650
Decision Date 1990-09-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

JOINT MOTON IMAGER(TM) received FDA 510(k) clearance under submission number K902583, sponsored by Concord Imaging, Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1990-09-27.

Classification & Regulation

This clearance is catalogued under FDA product code JAA and 21 CFR 892.1650, within the Radiology review panel as a Class II device.