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FDA 510(k)

DENTAL ALLOY

K-Number: K780090 · 1978-03-14

ApplicantKrupp International, Inc.
Decision Date1978-03-14
Product CodeEJH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DENTAL ALLOY is the device name listed in this FDA 510(k) record. The listed applicant is Krupp International, Inc.. It received FDA 510(k) clearance on 1978-03-14 under 510(k) number K780090. 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 DENTAL ALLOY?

DENTAL ALLOY is a medical device that received FDA 510(k) clearance on 1978-03-14. The listed applicant is Krupp International, Inc.. The 510(k) number is K780090.

When did DENTAL ALLOY receive FDA 510(k) clearance?

DENTAL ALLOY received FDA 510(k) clearance on 1978-03-14, under 510(k) number K780090.

Who is the listed applicant for DENTAL ALLOY?

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

What is the FDA product code for DENTAL ALLOY?

The FDA product code for DENTAL ALLOY is EJH.

Related Clinical Trials

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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Other records listing Krupp International, 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.

K800835KANDI-NUCLEAR MED. DATA ACQU.&INFO.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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