LUXACORE/LUXACORE DUAL— 510(k) K012307

Substantially Equivalent

Dmg USA, Inc.

FDA 510(k) clearance K012307 for LUXACORE/LUXACORE DUAL, Substantially Equivalent on 2001-08-23. Applicant: Dmg USA, Inc..

Clearance details

Applicant: Dmg USA, Inc.
Product code: Code EBF
Advisory panel: Dental
Date received: 2001-07-23
Decision date: 2001-08-23
Decision: Substantially Equivalent
Clearance type: Abbreviated
Location: Ayer, MA, US

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