RI-FORMER WALL MODEL 2,5 V/220 V OR 110 V 3,5 V/220 V OR 110 V, RI-FORMER ANAESTHETIC MODEL 2,5 V/220 V OR 110 C 3,5 V/V— 510(k) K950914

Name: FDA 510(k) clearance K950914
Creator: U.S. Food and Drug Administration
Published: 1995-07-24

Substantially Equivalent

Rudolf Riester GmbH & Co. KG

FDA 510(k) clearance K950914 for RI-FORMER WALL MODEL 2,5 V/220 V OR 110 V 3,5 V/220 V OR 110 V, RI-FORMER ANAESTHETIC MODEL 2,5 V/220 V OR 110 C 3,5 V/V, Substantially Equivalent on 1995-07-24. Applicant: Rudolf Riester GmbH & Co. KG. Device class: 2.

Clearance details

Applicant: Rudolf Riester GmbH & Co. KG
Product code: Code HLJ
Device class: Class 2
Regulation: 21 CFR 886.1570
Advisory panel: Ophthalmic
Date received: 1995-02-23
Decision date: 1995-07-24
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.