meddevicedb.com FDA Device Reference

VARIOUS AURAL GROMMETS

K812460 Class II Traditional
Decision Date
1981-09-21
Sponsor / Applicant
Exmoor Plastics , Ltd.

Technical Specification

510(k) Submission ID K812460
Product Code ETD
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.3880
Decision Date 1981-09-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VARIOUS AURAL GROMMETS received FDA 510(k) clearance under submission number K812460, sponsored by Exmoor Plastics , Ltd.. 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 1981-09-21.

Classification & Regulation

This clearance is catalogued under FDA product code ETD and 21 CFR 874.3880, within the Ear, Nose, Throat review panel as a Class II device.