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ENT-2 FLEXIBLE NASOPHARYGNO-LARYNGOSCOPES

K900176 Class II Traditional
Decision Date
1990-04-10
Sponsor / Applicant
Machida, Inc.

Technical Specification

510(k) Submission ID K900176
Product Code EOB
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.4760
Decision Date 1990-04-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ENT-2 FLEXIBLE NASOPHARYGNO-LARYNGOSCOPES received FDA 510(k) clearance under submission number K900176, sponsored by Machida, Inc.. 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 1990-04-10.

Classification & Regulation

This clearance is catalogued under FDA product code EOB and 21 CFR 874.4760, within the Ear, Nose, Throat review panel as a Class II device.