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FDA 510(k)

DEGUCAST 40

K-Number: K922790 · 1992-12-03

ApplicantDegussa AG
Decision Date1992-12-03
Product CodeEJH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DEGUCAST 40 is the device name listed in this FDA 510(k) record. The listed applicant is Degussa AG. It received FDA 510(k) clearance on 1992-12-03 under 510(k) number K922790. 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 DEGUCAST 40?

DEGUCAST 40 is a medical device that received FDA 510(k) clearance on 1992-12-03. The listed applicant is Degussa AG. The 510(k) number is K922790.

When did DEGUCAST 40 receive FDA 510(k) clearance?

DEGUCAST 40 received FDA 510(k) clearance on 1992-12-03, under 510(k) number K922790.

Who is the listed applicant for DEGUCAST 40?

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

What is the FDA product code for DEGUCAST 40?

The FDA product code for DEGUCAST 40 is EJH.

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Other records listing Degussa AG 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.

K953344DEGUBOND ULTRAK931808DUCERAGOLD, DUCERATINK926347DUCERANIUM UK921772BIOLORK921479DUCERATIN/DUCERAM LFC DENTAL PORCELAINK921445DEGUBOND PLUS

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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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