UNI II— 510(k) K925756

Substantially Equivalent

Rudolf Riester GmbH & Co. KG

FDA 510(k) clearance K925756 for UNI II, Substantially Equivalent on 1993-10-18. 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: 1992-11-13
Decision date: 1993-10-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: D-72417 Jungingen, DE

Download summary PDF View on FDA.gov ↗

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K972378 — SANAPHON N1997-09-24
K972379 — PRECISA N1997-09-24

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