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FDA 510(k)

KAVO EVEREST ZH-BLANK

K-Number: K033221 · 2003-10-28

ApplicantKavo America Corporation
Decision Date2003-10-28
Product CodeEIH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

KAVO EVEREST ZH-BLANK is the device name listed in this FDA 510(k) record. The listed applicant is Kavo America Corporation. It received FDA 510(k) clearance on 2003-10-28 under 510(k) number K033221. 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 KAVO EVEREST ZH-BLANK?

KAVO EVEREST ZH-BLANK is a medical device that received FDA 510(k) clearance on 2003-10-28. The listed applicant is Kavo America Corporation. The 510(k) number is K033221.

When did KAVO EVEREST ZH-BLANK receive FDA 510(k) clearance?

KAVO EVEREST ZH-BLANK received FDA 510(k) clearance on 2003-10-28, under 510(k) number K033221.

Who is the listed applicant for KAVO EVEREST ZH-BLANK?

The FDA 510(k) record lists Kavo America Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KAVO EVEREST ZH-BLANK?

The FDA product code for KAVO EVEREST ZH-BLANK is EIH.

Related Clinical Trials

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Other records listing Kavo America Corporation 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.

K042394DIAGNODENT PERIO TIP (ACCESSORY)K050744KAVO ERGOCOM/ERGOCAMK042872RONDOFLEX PLUS 360

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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