GEISTLICH PERIO-SYSTEM COMBI-PACK , GEISTLICH BIO-GIDE PERIO— 510(k) K112575

Name: FDA 510(k) clearance K112575
Creator: U.S. Food and Drug Administration
Published: 2011-12-27

Substantially Equivalent

Geistlich Pharma AG

FDA 510(k) clearance K112575 for GEISTLICH PERIO-SYSTEM COMBI-PACK , GEISTLICH BIO-GIDE PERIO, Substantially Equivalent on 2011-12-27. Applicant: Geistlich Pharma AG. Device class: 2.

Clearance details

Applicant: Geistlich Pharma AG
Product code: Code NPM
Device class: Class 2
Regulation: 21 CFR 872.3930
Advisory panel: Dental
Date received: 2011-09-06
Decision date: 2011-12-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

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