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IMAGE STAR II

K052610 Class II Traditional
Decision Date
2005-11-30
Sponsor / Applicant
Lakeshore Technologies, Inc.

Technical Specification

510(k) Submission ID K052610
Product Code JAA
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1650
Decision Date 2005-11-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IMAGE STAR II received FDA 510(k) clearance under submission number K052610, sponsored by Lakeshore Technologies, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2005-11-30.

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.