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FDA 510(k)

KAVO EVEREST TITANBLANK

K-Number: K024214 · 2003-03-12

ApplicantKavo America
Decision Date2003-03-12
Product CodeEJH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

KAVO EVEREST TITANBLANK is the device name listed in this FDA 510(k) record. The listed applicant is Kavo America. It received FDA 510(k) clearance on 2003-03-12 under 510(k) number K024214. The device is classified under product code EJH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KAVO EVEREST TITANBLANK?

KAVO EVEREST TITANBLANK is a medical device that received FDA 510(k) clearance on 2003-03-12. The listed applicant is Kavo America. The 510(k) number is K024214.

When did KAVO EVEREST TITANBLANK receive FDA 510(k) clearance?

KAVO EVEREST TITANBLANK received FDA 510(k) clearance on 2003-03-12, under 510(k) number K024214.

Who is the listed applicant for KAVO EVEREST TITANBLANK?

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

What is the FDA product code for KAVO EVEREST TITANBLANK?

The FDA product code for KAVO EVEREST TITANBLANK is EJH.

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Other records listing Kavo America 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.

K073074KEY LASER III 1243 US WITH DETECTK072262GENTLERAY 980 DIODE LASER SYSTEMK063624KAVO EVEREST C-TEMPK051909DIAGNODENTK030146KAVO KEY LASER 1242 AND KAVO KEY LASER 1243+K050019IN EXAM INTRAORAL DENTAL X-RAY SYSTEM

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Related Devices (Code: EJH)

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.

K123929BEGOPAL+Bego Bremer Goldschlaegerei Wilh. Herbst GmbH & COK040180CONTINUM VAalba Dent, Inc.K040179CONTINUMAalba Dent, Inc.K033356VERASOFT ESAalba Dent, Inc.K033045DREAM BOND, DREAMCAST CHROME, DREAMCAST V, DREAM FLEXICAST, DREAM LITHECASTAmerican Green Dent. Mfg, Inc.K032136WIROBOND CBego U.S.A.

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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