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DISPOSABLE SILICONE EPISTAXIS CATHETER

K973656 Class I Traditional
Decision Date
1997-11-18
Sponsor / Applicant
Specialty Surgical Products, Inc.

Technical Specification

510(k) Submission ID K973656
Product Code EMX
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.4100
Decision Date 1997-11-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DISPOSABLE SILICONE EPISTAXIS CATHETER received FDA 510(k) clearance under submission number K973656, sponsored by Specialty Surgical Products, 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 1997-11-18.

Classification & Regulation

This clearance is catalogued under FDA product code EMX and 21 CFR 874.4100, within the Ear, Nose, Throat review panel as a Class I device.