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INSTRUMENT CABINET

K833882 Class I Traditional
Decision Date
1984-01-27
Sponsor / Applicant
Jedmed Instrument Co.

Technical Specification

510(k) Submission ID K833882
Product Code ETF
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.5300
Decision Date 1984-01-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

INSTRUMENT CABINET received FDA 510(k) clearance under submission number K833882, sponsored by Jedmed Instrument Co.. 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 1984-01-27.

Classification & Regulation

This clearance is catalogued under FDA product code ETF and 21 CFR 874.5300, within the Ear, Nose, Throat review panel as a Class I device.