KING-HUE, ROYAL CORAL, SUPER-C ARTIFICIAL TEETH
K-Number: K931162 · 1993-05-27
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Device Summary
Frequently Asked Questions
What is the KING-HUE, ROYAL CORAL, SUPER-C ARTIFICIAL TEETH?
KING-HUE, ROYAL CORAL, SUPER-C ARTIFICIAL TEETH is a medical device that received FDA 510(k) clearance on 1993-05-27. The listed applicant is King Dental Corp.. The 510(k) number is K931162.
When did KING-HUE, ROYAL CORAL, SUPER-C ARTIFICIAL TEETH receive FDA 510(k) clearance?
KING-HUE, ROYAL CORAL, SUPER-C ARTIFICIAL TEETH received FDA 510(k) clearance on 1993-05-27, under 510(k) number K931162.
Who is the listed applicant for KING-HUE, ROYAL CORAL, SUPER-C ARTIFICIAL TEETH?
The FDA 510(k) record lists King Dental Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for KING-HUE, ROYAL CORAL, SUPER-C ARTIFICIAL TEETH?
The FDA product code for KING-HUE, ROYAL CORAL, SUPER-C ARTIFICIAL TEETH is ELM.
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 King Dental 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: ELM)
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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