meddevicedb.com FDA Device Reference

COMPACT LASER IMAGER, MODEL CLI-100

K902347 Class II Traditional
Decision Date
1991-03-04
Sponsor / Applicant
Lumisys, Inc.

Technical Specification

510(k) Submission ID K902347
Product Code LMC
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.2040
Decision Date 1991-03-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

COMPACT LASER IMAGER, MODEL CLI-100 received FDA 510(k) clearance under submission number K902347, sponsored by Lumisys, 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 1991-03-04.

Classification & Regulation

This clearance is catalogued under FDA product code LMC and 21 CFR 892.2040, within the Radiology review panel as a Class II device.