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FDA 510(k)

NEKO CERAMIC CONVENIENCE CROWNS

K-Number: K771128 · 1977-07-15

Decision Date1977-07-15
Product CodeELZ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

NEKO CERAMIC CONVENIENCE CROWNS is the device name listed in this FDA 510(k) record. The listed applicant is Sterndent Corp.. It received FDA 510(k) clearance on 1977-07-15 under 510(k) number K771128. The device is classified under product code ELZ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEKO CERAMIC CONVENIENCE CROWNS?

NEKO CERAMIC CONVENIENCE CROWNS is a medical device that received FDA 510(k) clearance on 1977-07-15. The listed applicant is Sterndent Corp.. The 510(k) number is K771128.

When did NEKO CERAMIC CONVENIENCE CROWNS receive FDA 510(k) clearance?

NEKO CERAMIC CONVENIENCE CROWNS received FDA 510(k) clearance on 1977-07-15, under 510(k) number K771128.

Who is the listed applicant for NEKO CERAMIC CONVENIENCE CROWNS?

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

What is the FDA product code for NEKO CERAMIC CONVENIENCE CROWNS?

The FDA product code for NEKO CERAMIC CONVENIENCE CROWNS is ELZ.

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 Sterndent Corp. 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: ELZ)

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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