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MILLENNIUM III 3T-8-CHANNEL NEUROVASCULAR COIL

K042342 Class II Special
Decision Date
2004-09-24
Sponsor / Applicant
Usa Instruments, Inc.

Technical Specification

510(k) Submission ID K042342
Product Code MOS
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1000
Decision Date 2004-09-24
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MILLENNIUM III 3T-8-CHANNEL NEUROVASCULAR COIL received FDA 510(k) clearance under submission number K042342, sponsored by Usa Instruments, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2004-09-24.

Classification & Regulation

This clearance is catalogued under FDA product code MOS and 21 CFR 892.1000, within the Radiology review panel as a Class II device.