meddevicedb.com FDA Device Reference

PINNACLE MAGNETIC RESONANCE IMAGING SCANNER

K011485 Class II Special
Decision Date
2001-06-06
Sponsor / Applicant
Fonar Corp.

Technical Specification

510(k) Submission ID K011485
Product Code LNH
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1000
Decision Date 2001-06-06
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PINNACLE MAGNETIC RESONANCE IMAGING SCANNER received FDA 510(k) clearance under submission number K011485, sponsored by Fonar Corp.. The device was reviewed via the Special premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2001-06-06.

Classification & Regulation

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