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FDA 510(k)

BEGOPAL+

K-Number: K123929 · 2013-03-14

ApplicantBego Bremer Goldschlaegerei Wilh. Herbst GmbH & CO
Decision Date2013-03-14
Product CodeEJH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

BEGOPAL+ is the device name listed in this FDA 510(k) record. The listed applicant is Bego Bremer Goldschlaegerei Wilh. Herbst GmbH & CO. It received FDA 510(k) clearance on 2013-03-14 under 510(k) number K123929. 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 BEGOPAL+?

BEGOPAL+ is a medical device that received FDA 510(k) clearance on 2013-03-14. The listed applicant is Bego Bremer Goldschlaegerei Wilh. Herbst GmbH & CO. The 510(k) number is K123929.

When did BEGOPAL+ receive FDA 510(k) clearance?

BEGOPAL+ received FDA 510(k) clearance on 2013-03-14, under 510(k) number K123929.

Who is the listed applicant for BEGOPAL+?

The FDA 510(k) record lists Bego Bremer Goldschlaegerei Wilh. Herbst GmbH & CO as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BEGOPAL+?

The FDA product code for BEGOPAL+ is EJH.

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Other records listing Bego Bremer Goldschlaegerei Wilh. Herbst GmbH & CO 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.

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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.

K040180CONTINUM 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.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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