DRFP PROSMART ROOT CANAL OBTURATION SYSTEM, PROPOINTS 4% 6%, PT, S— 510(k) K100248

Name: FDA 510(k) clearance K100248
Creator: U.S. Food and Drug Administration
Published: 2010-10-22

Substantially Equivalent

Drfp , Ltd.

FDA 510(k) clearance K100248 for DRFP PROSMART ROOT CANAL OBTURATION SYSTEM, PROPOINTS 4% 6%, PT, S, Substantially Equivalent on 2010-10-22. Applicant: Drfp , Ltd.. Device class: 2.

Clearance details

Applicant: Drfp , Ltd.
Product code: Code KIF
Device class: Class 2
Regulation: 21 CFR 872.3820
Advisory panel: Dental
Date received: 2010-01-27
Decision date: 2010-10-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Amsterdam, Nh, NL

Download summary PDF View on FDA.gov ↗

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