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FDA 510(k)

VITA VMK MASTER

K-Number: K093446 · 2009-12-03

ApplicantVita Zahnfabrik H. Rauter GmbH & Co. Kg.
Decision Date2009-12-03
Product CodeEIH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

VITA VMK MASTER is the device name listed in this FDA 510(k) record. The listed applicant is Vita Zahnfabrik H. Rauter GmbH & Co. Kg.. It received FDA 510(k) clearance on 2009-12-03 under 510(k) number K093446. The device is classified under product code EIH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VITA VMK MASTER?

VITA VMK MASTER is a medical device that received FDA 510(k) clearance on 2009-12-03. The listed applicant is Vita Zahnfabrik H. Rauter GmbH & Co. Kg.. The 510(k) number is K093446.

When did VITA VMK MASTER receive FDA 510(k) clearance?

VITA VMK MASTER received FDA 510(k) clearance on 2009-12-03, under 510(k) number K093446.

Who is the listed applicant for VITA VMK MASTER?

The FDA 510(k) record lists Vita Zahnfabrik H. Rauter GmbH & Co. Kg. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VITA VMK MASTER?

The FDA product code for VITA VMK MASTER is EIH.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Other records listing Vita Zahnfabrik H. Rauter GmbH & Co. Kg. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K251587VITA VMLC Primer

Related Devices (Code: EIH)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K262074Any-ZircosMediclus Co., Ltd.K262239Obsidian® Press Over ZirconiaPrismatik Dentalcraft, Inc.K261046Dental Zirconia Blank & Coloring LiquidHunan Qinghao Puzhong Technology Co., Ltd.K262195Dandy Ceramic Stain and GlazeZima International Inc., dba DandyK260918Zolid LunarisAmann Girrbach AGK260859Rosetta SM, Rosetta SPHass Corp.

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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