meddevicedb.com FDA Device Reference

NOBLE MODEL DOUBLESIDED TREATMENT UNIT

K801739 Class I Traditional
Decision Date
1980-08-13
Sponsor / Applicant
Jedmed Instrument Co.

Technical Specification

510(k) Submission ID K801739
Product Code ETF
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.5300
Decision Date 1980-08-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NOBLE MODEL DOUBLESIDED TREATMENT UNIT received FDA 510(k) clearance under submission number K801739, 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 1980-08-13.

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.