meddevicedb.com FDA Device Reference

1.0T 8-CHANNEL PANORAMA BREAST ARRAY COIL

K093284 Class II Traditional
Decision Date
2010-02-01
Sponsor / Applicant
Invivo Corporation

Technical Specification

510(k) Submission ID K093284
Product Code MOS
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1000
Decision Date 2010-02-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

1.0T 8-CHANNEL PANORAMA BREAST ARRAY COIL received FDA 510(k) clearance under submission number K093284, sponsored by Invivo 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 2010-02-01.

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.