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FDA 510(k)

CERGOGOLD

K-Number: K993897 · 2000-01-10

Decision Date2000-01-10
Product CodeEIH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CERGOGOLD is the device name listed in this FDA 510(k) record. The listed applicant is Degussa - Ney Dental, Inc.. It received FDA 510(k) clearance on 2000-01-10 under 510(k) number K993897. The device is classified under product code EIH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CERGOGOLD?

CERGOGOLD is a medical device that received FDA 510(k) clearance on 2000-01-10. The listed applicant is Degussa - Ney Dental, Inc.. The 510(k) number is K993897.

When did CERGOGOLD receive FDA 510(k) clearance?

CERGOGOLD received FDA 510(k) clearance on 2000-01-10, under 510(k) number K993897.

Who is the listed applicant for CERGOGOLD?

The FDA 510(k) record lists Degussa - Ney Dental, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CERGOGOLD?

The FDA product code for CERGOGOLD is EIH.

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.

Other records listing Degussa - Ney Dental, 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.

Related Devices (Code: EIH)

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.

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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