PORTA REFLEX— 510(k) K040672

Name: FDA 510(k) clearance K040672
Creator: U.S. Food and Drug Administration
Published: 2004-05-27

Substantially Equivalent

Wieland Dental + Technik GmbH & Co. KG

FDA 510(k) clearance K040672 for PORTA REFLEX, Substantially Equivalent on 2004-05-27. Applicant: Wieland Dental + Technik GmbH & Co. KG. Device class: 2.

Clearance details

Applicant: Wieland Dental + Technik GmbH & Co. KG
Product code: Code EJT
Device class: Class 2
Regulation: 21 CFR 872.3060
Advisory panel: Dental
Date received: 2004-03-15
Decision date: 2004-05-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Pforzheim, DE

Download summary PDF View on FDA.gov ↗

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