LUXATEMP AUTOMIX— 510(k) K924830

Name: FDA 510(k) clearance K924830
Creator: U.S. Food and Drug Administration
Published: 1994-04-29

Substantially Equivalent

Dmg Chemisch Pharmazeutische Fabrik GmbH

FDA 510(k) clearance K924830 for LUXATEMP AUTOMIX, Substantially Equivalent on 1994-04-29. Applicant: Dmg Chemisch Pharmazeutische Fabrik GmbH. Device class: 2.

Clearance details

Applicant: Dmg Chemisch Pharmazeutische Fabrik GmbH
Product code: Code EBG
Device class: Class 2
Regulation: 21 CFR 872.3770
Advisory panel: Dental
Date received: 1992-09-25
Decision date: 1994-04-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Germany, GR

Download summary PDF View on FDA.gov ↗

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