IONOSCEM OR IONOSCELL GLASS IONOMER DENTAL CEMENT— 510(k) K881661

Name: FDA 510(k) clearance K881661
Creator: U.S. Food and Drug Administration
Published: 1988-06-07

Substantially Equivalent

Specialites Septodont

FDA 510(k) clearance K881661 for IONOSCEM OR IONOSCELL GLASS IONOMER DENTAL CEMENT, Substantially Equivalent on 1988-06-07. Applicant: Specialites Septodont. Device class: 2.

Clearance details

Applicant: Specialites Septodont
Product code: Code EMA
Device class: Class 2
Regulation: 21 CFR 872.3275
Advisory panel: Dental
Date received: 1988-04-15
Decision date: 1988-06-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, 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.