CERASORB DENTAL, CERASORB M DENTAL AND CERASORB PERIO— 510(k) K051443

Name: FDA 510(k) clearance K051443
Creator: U.S. Food and Drug Administration
Published: 2005-07-22

Substantially Equivalent

Curasan Ag, Frankfurt Facility

FDA 510(k) clearance K051443 for CERASORB DENTAL, CERASORB M DENTAL AND CERASORB PERIO, Substantially Equivalent on 2005-07-22. Applicant: Curasan Ag, Frankfurt Facility. Device class: 2.

Clearance details

Applicant: Curasan Ag, Frankfurt Facility
Product code: Code LYC
Device class: Class 2
Regulation: 21 CFR 872.3930
Advisory panel: Dental
Date received: 2005-06-02
Decision date: 2005-07-22
Decision: Substantially Equivalent
Clearance type: Abbreviated
Location: Garner,, NC, US

Download summary PDF View on FDA.gov ↗

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