MODI. OF DENTAL CERAMIC FOR FABRICATION OF CROWN
K-Number: K864724 · 1987-02-17
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Device Summary
Frequently Asked Questions
What is the MODI. OF DENTAL CERAMIC FOR FABRICATION OF CROWN?
MODI. OF DENTAL CERAMIC FOR FABRICATION OF CROWN is a medical device that received FDA 510(k) clearance on 1987-02-17. The listed applicant is Dentsply Intl.. The 510(k) number is K864724.
When did MODI. OF DENTAL CERAMIC FOR FABRICATION OF CROWN receive FDA 510(k) clearance?
MODI. OF DENTAL CERAMIC FOR FABRICATION OF CROWN received FDA 510(k) clearance on 1987-02-17, under 510(k) number K864724.
Who is the listed applicant for MODI. OF DENTAL CERAMIC FOR FABRICATION OF CROWN?
The FDA 510(k) record lists Dentsply Intl. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MODI. OF DENTAL CERAMIC FOR FABRICATION OF CROWN?
The FDA product code for MODI. OF DENTAL CERAMIC FOR FABRICATION OF CROWN is ELL.
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 Dentsply Intl. 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: ELL)
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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