meddevicedb.com FDA Device Reference

ULTRASTAT NASAL CATHETER

K901310 Class I Traditional
Decision Date
1990-06-14
Sponsor / Applicant
Invotec International, Inc.

Technical Specification

510(k) Submission ID K901310
Product Code EMX
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.4100
Decision Date 1990-06-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ULTRASTAT NASAL CATHETER received FDA 510(k) clearance under submission number K901310, sponsored by Invotec International, 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 1990-06-14.

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.