meddevicedb.com FDA Device Reference

41-180 TO 41-246 VARIOUS NASAL FORCEPS

K851794 Class I Traditional
Decision Date
1985-06-11
Sponsor / Applicant
Artiberia

Technical Specification

510(k) Submission ID K851794
Product Code KAE
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.4420
Decision Date 1985-06-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

41-180 TO 41-246 VARIOUS NASAL FORCEPS received FDA 510(k) clearance under submission number K851794, sponsored by Artiberia. 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 1985-06-11.

Classification & Regulation

This clearance is catalogued under FDA product code KAE and 21 CFR 874.4420, within the Ear, Nose, Throat review panel as a Class I device.