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FDA 510(k)

CONTINUM V

K-Number: K040180 · 2004-03-04

ApplicantAalba Dent, Inc.
Decision Date2004-03-04
Product CodeEJH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CONTINUM V is the device name listed in this FDA 510(k) record. The listed applicant is Aalba Dent, Inc.. It received FDA 510(k) clearance on 2004-03-04 under 510(k) number K040180. 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 CONTINUM V?

CONTINUM V is a medical device that received FDA 510(k) clearance on 2004-03-04. The listed applicant is Aalba Dent, Inc.. The 510(k) number is K040180.

When did CONTINUM V receive FDA 510(k) clearance?

CONTINUM V received FDA 510(k) clearance on 2004-03-04, under 510(k) number K040180.

Who is the listed applicant for CONTINUM V?

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

What is the FDA product code for CONTINUM V?

The FDA product code for CONTINUM V is EJH.

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Other records listing Aalba Dent, Inc. 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.

K040179CONTINUMK033356VERASOFT ESK982094VERABOND 2K972971NPG + 2K973265VERABOND 2VK972607PLATALLOY

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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 & COK040179CONTINUMAalba 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.K031627NANO-TICROWNNano-Write 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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