UNI I— 510(k) K925759

Substantially Equivalent

Rudolf Riester GmbH & Co. KG

FDA 510(k) clearance K925759 for UNI I, Substantially Equivalent on 1993-07-26. Applicant: Rudolf Riester GmbH & Co. KG. Device class: 1.

Clearance details

Applicant: Rudolf Riester GmbH & Co. KG
Product code: Code ERA
Device class: Class 1
Regulation: 21 CFR 874.4770
Advisory panel: Ear, Nose, Throat
Date received: 1992-11-13
Decision date: 1993-07-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: D-72417 Jungingen, DE

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Data sourced from openFDA. This site is unofficial and independent of the FDA.