CERASORB DENTAL,CERADORB M DENTAL, CERASORB PERIO— 510(k) K113282

Name: FDA 510(k) clearance K113282
Creator: U.S. Food and Drug Administration
Published: 2012-09-20

Substantially Equivalent

Riemser Arzeimittel AG

FDA 510(k) clearance K113282 for CERASORB DENTAL,CERADORB M DENTAL, CERASORB PERIO, Substantially Equivalent on 2012-09-20. Applicant: Riemser Arzeimittel AG. Device class: 2.

Clearance details

Applicant: Riemser Arzeimittel AG
Product code: Code LYC
Device class: Class 2
Regulation: 21 CFR 872.3930
Advisory panel: Dental
Date received: 2011-11-07
Decision date: 2012-09-20
Decision: Substantially Equivalent
Clearance type: Special
Location: Durham, 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.