CERASORB PLUS— 510(k) K120152

Substantially Equivalent

Riemser Arzneimittel AG

FDA 510(k) clearance K120152 for CERASORB PLUS, Substantially Equivalent on 2012-08-13. Applicant: Riemser Arzneimittel AG. Device class: 2.

Clearance details

Applicant: Riemser Arzneimittel AG
Product code: Code NPM
Device class: Class 2
Regulation: 21 CFR 872.3930
Advisory panel: Dental
Date received: 2012-01-18
Decision date: 2012-08-13
Decision: Substantially Equivalent
Clearance type: Abbreviated
Location: Durham, NC, US

Download summary PDF View on FDA.gov ↗

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