SIMIDUR S2— 510(k) K020192

Name: FDA 510(k) clearance K020192
Creator: U.S. Food and Drug Administration
Published: 2002-03-15

Substantially Equivalent

Wieland Dental + Technik GmbH & Co. KG

FDA 510(k) clearance K020192 for SIMIDUR S2, Substantially Equivalent on 2002-03-15. Applicant: Wieland Dental + Technik GmbH & Co. KG. Device class: 2.

Clearance details

Applicant: Wieland Dental + Technik GmbH & Co. KG
Product code: Code EJS
Device class: Class 2
Regulation: 21 CFR 872.3060
Advisory panel: Dental
Date received: 2002-01-22
Decision date: 2002-03-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Pforzheim, DE

Download summary PDF View on FDA.gov ↗

Recent devices under product code EJS

view all

K041433 — BRIGHT GOLD XH2004-08-19
K040436 — SIMIDUR SUPERIOR2004-03-05
K022252 — STERNGOLD 1, MODEL 11277812002-09-19
K022469 — ECO E42002-09-18
K021367 — STERNGOLD 66, MODEL #11802302002-05-16

More clearances from Wieland Dental + Technik GmbH & Co. KG

view all

K152118 — Zenostar MT, Zenostar Color Liquids2015-12-16
K151142 — IVOBASE CAD FOR ZENOTEC, IVOBASE CAD BOND, IVOBASE CAD MODELLING LIQUID2015-08-13
K142233 — zenostar MO, Zenostar T, Zenostar VisualiZr2015-01-05
K130184 — ZENOLUX2013-05-24
K112710 — ZENOTEC ZR BRIDGE, ZENOSTAR ZR TRANSLUCENT, ZENOTEC COLOR ZR, ZENOSTAR COLOR ZR2011-10-17

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