LUXAGLAZE— 510(k) K013179

Substantially Equivalent

Dmg USA, Inc.

FDA 510(k) clearance K013179 for LUXAGLAZE, Substantially Equivalent on 2001-10-12. Applicant: Dmg USA, Inc..

Clearance details

Applicant: Dmg USA, Inc.
Product code: Code EBD
Advisory panel: Dental
Date received: 2001-09-24
Decision date: 2001-10-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Dover, DE, US

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