meddevicedb.com FDA Device Reference

INSTANT IN-DWELL NASAL SUCT TAMP/ALLEVIA NASAL TRA

K924944 Class I Traditional
Decision Date
1993-07-02
Sponsor / Applicant
Westmed Intl.

Technical Specification

510(k) Submission ID K924944
Product Code EMX
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.4100
Decision Date 1993-07-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

INSTANT IN-DWELL NASAL SUCT TAMP/ALLEVIA NASAL TRA received FDA 510(k) clearance under submission number K924944, sponsored by Westmed Intl.. 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 1993-07-02.

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.