meddevicedb.com FDA Device Reference

PERFECT, ENT SET, PRAKTIKANT, DE LUXE

K950913 Class I Traditional
Decision Date
1995-05-12
Sponsor / Applicant
Rudolf Riester GmbH & Co. KG

Technical Specification

510(k) Submission ID K950913
Product Code ERA
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.4770
Decision Date 1995-05-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PERFECT, ENT SET, PRAKTIKANT, DE LUXE received FDA 510(k) clearance under submission number K950913, sponsored by Rudolf Riester GmbH & Co. KG. 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 1995-05-12.

Classification & Regulation

This clearance is catalogued under FDA product code ERA and 21 CFR 874.4770, within the Ear, Nose, Throat review panel as a Class I device.