NEKO CERAMIC CONVENIENCE CROWNS
K-Number: K771128 · 1977-07-15
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Device Summary
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
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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