meddevicedb.com FDA Device Reference

BRIMFIELD FIBEROPTIC LIGHT SCOURCE

K841731 Class I Traditional
Decision Date
1984-07-16
Sponsor / Applicant
Brimfield Scientific Instruments

Technical Specification

510(k) Submission ID K841731
Product Code EQH
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.4350
Decision Date 1984-07-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BRIMFIELD FIBEROPTIC LIGHT SCOURCE received FDA 510(k) clearance under submission number K841731, sponsored by Brimfield Scientific Instruments. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ear, Nose, Throat review panel. The statutory decision date of record is 1984-07-16.

Classification & Regulation

This clearance is catalogued under FDA product code EQH and 21 CFR 874.4350, within the Ear, Nose, Throat review panel as a Class I device.