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SILICONE BLOCK

K042380 Class II Traditional
Decision Date
2004-10-25
Sponsor / Applicant
National Medical Devices, Inc.

Technical Specification

510(k) Submission ID K042380
Product Code MIB
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.3620
Decision Date 2004-10-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SILICONE BLOCK received FDA 510(k) clearance under submission number K042380, sponsored by National Medical Devices, 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 2004-10-25.

Classification & Regulation

This clearance is catalogued under FDA product code MIB and 21 CFR 874.3620, within the Ear, Nose, Throat review panel as a Class II device.