CERACELL DENTAL— 510(k) K103709

Substantially Equivalent

Curasan AG

FDA 510(k) clearance K103709 for CERACELL DENTAL, Substantially Equivalent on 2011-03-10. Applicant: Curasan AG. Device class: 2.

Clearance details

Applicant: Curasan AG
Product code: Code LYC
Device class: Class 2
Regulation: 21 CFR 872.3930
Advisory panel: Dental
Date received: 2010-12-20
Decision date: 2011-03-10
Decision: Substantially Equivalent
Clearance type: Abbreviated
Location: Rome, IT

Download summary PDF View on FDA.gov ↗

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