FLOWABLE COMPOSITE/ ECUFLOW/ LUXAFLOW— 510(k) K011211

Name: FDA 510(k) clearance K011211
Creator: U.S. Food and Drug Administration
Published: 2001-06-18

Substantially Equivalent

Dmg USA, Inc.

FDA 510(k) clearance K011211 for FLOWABLE COMPOSITE/ ECUFLOW/ LUXAFLOW, Substantially Equivalent on 2001-06-18. Applicant: Dmg USA, Inc.. Device class: 2.

Clearance details

Applicant: Dmg USA, Inc.
Product code: Code EBF
Device class: Class 2
Regulation: 21 CFR 872.3690
Advisory panel: Dental
Date received: 2001-04-19
Decision date: 2001-06-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ayer, MA, 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.