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FDA 510(k)

LUXAGLAZE

K-Number: K013179 · 2001-10-12

ApplicantDmg USA, Inc.
Decision Date2001-10-12
Product CodeEBD
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

LUXAGLAZE is the device name listed in this FDA 510(k) record. The listed applicant is Dmg USA, Inc.. It received FDA 510(k) clearance on 2001-10-12 under 510(k) number K013179. The device is classified under product code EBD. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LUXAGLAZE?

LUXAGLAZE is a medical device that received FDA 510(k) clearance on 2001-10-12. The listed applicant is Dmg USA, Inc.. The 510(k) number is K013179.

When did LUXAGLAZE receive FDA 510(k) clearance?

LUXAGLAZE received FDA 510(k) clearance on 2001-10-12, under 510(k) number K013179.

Who is the listed applicant for LUXAGLAZE?

The FDA 510(k) record lists Dmg USA, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LUXAGLAZE?

The FDA product code for LUXAGLAZE is EBD.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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