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NASAL-SINUS PACKING

K924542 Class I Traditional
Decision Date
1993-02-12
Sponsor / Applicant
Ultracell Medical Technologies, Inc.

Technical Specification

510(k) Submission ID K924542
Product Code EMX
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.4100
Decision Date 1993-02-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NASAL-SINUS PACKING received FDA 510(k) clearance under submission number K924542, sponsored by Ultracell Medical Technologies, 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 1993-02-12.

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.