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ENTITY NASOVIEW LED NASOPHARYNGOSCOPE, MODEL 006105

K080622 Class II Special
Decision Date
2008-04-02
Sponsor / Applicant
Optim, Inc.

Technical Specification

510(k) Submission ID K080622
Product Code EOB
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.4760
Decision Date 2008-04-02
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ENTITY NASOVIEW LED NASOPHARYNGOSCOPE, MODEL 006105 received FDA 510(k) clearance under submission number K080622, sponsored by Optim, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Ear, Nose, Throat review panel. The statutory decision date of record is 2008-04-02.

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.