meddevicedb.com FDA Device Reference

13-320,13-330 TWO TYPES NAZAL SCISSORS-HEYMAN,BECK

K851763 Class I Traditional
Decision Date
1985-06-11
Sponsor / Applicant
Artiberia

Technical Specification

510(k) Submission ID K851763
Product Code KBD
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

13-320,13-330 TWO TYPES NAZAL SCISSORS-HEYMAN,BECK received FDA 510(k) clearance under submission number K851763, 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 KBD and 21 CFR 874.4420, within the Ear, Nose, Throat review panel as a Class I device.