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LAMP, FLOURESCENT BLACK, HIGH OUTPUT

K760471 Class II Traditional
Decision Date
1976-09-15
Sponsor / Applicant
Dermatron Corp.

Technical Specification

510(k) Submission ID K760471
Product Code FTC
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4630
Decision Date 1976-09-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LAMP, FLOURESCENT BLACK, HIGH OUTPUT received FDA 510(k) clearance under submission number K760471, sponsored by Dermatron Corp.. 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 1976-09-15.

Classification & Regulation

This clearance is catalogued under FDA product code FTC and 21 CFR 878.4630, within the General, Plastic Surgery review panel as a Class II device.