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FILMLESS CLINIC

K031704 Class II Abbreviated
Decision Date
2003-07-31
Sponsor / Applicant
Connect Imaging, Inc.

Technical Specification

510(k) Submission ID K031704
Product Code LLZ
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.2050
Decision Date 2003-07-31
Clearance Pathway Abbreviated

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FILMLESS CLINIC received FDA 510(k) clearance under submission number K031704, sponsored by Connect Imaging, Inc.. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2003-07-31.

Classification & Regulation

This clearance is catalogued under FDA product code LLZ and 21 CFR 892.2050, within the Radiology review panel as a Class II device.