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MI-15 EXAM SURGICAL LIGHT

K930897 Class II Traditional
Decision Date
1993-06-25
Sponsor / Applicant
Medical Illumination, Inc.

Technical Specification

510(k) Submission ID K930897
Product Code FTD
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4580
Decision Date 1993-06-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MI-15 EXAM SURGICAL LIGHT received FDA 510(k) clearance under submission number K930897, sponsored by Medical Illumination, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 1993-06-25.

Classification & Regulation

This clearance is catalogued under FDA product code FTD and 21 CFR 878.4580, within the General, Plastic Surgery review panel as a Class II device.