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FDA 510(k)

DICOR CASTABLE CERAMIC-ALL PORCELAIN BRIDGES

K-Number: K853707 · 1985-11-19

ApplicantDentsply Intl.
Decision Date1985-11-19
Product CodeEIH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DICOR CASTABLE CERAMIC-ALL PORCELAIN BRIDGES is the device name listed in this FDA 510(k) record. The listed applicant is Dentsply Intl.. It received FDA 510(k) clearance on 1985-11-19 under 510(k) number K853707. 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 DICOR CASTABLE CERAMIC-ALL PORCELAIN BRIDGES?

DICOR CASTABLE CERAMIC-ALL PORCELAIN BRIDGES is a medical device that received FDA 510(k) clearance on 1985-11-19. The listed applicant is Dentsply Intl.. The 510(k) number is K853707.

When did DICOR CASTABLE CERAMIC-ALL PORCELAIN BRIDGES receive FDA 510(k) clearance?

DICOR CASTABLE CERAMIC-ALL PORCELAIN BRIDGES received FDA 510(k) clearance on 1985-11-19, under 510(k) number K853707.

Who is the listed applicant for DICOR CASTABLE CERAMIC-ALL PORCELAIN BRIDGES?

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 DICOR CASTABLE CERAMIC-ALL PORCELAIN BRIDGES?

The FDA product code for DICOR CASTABLE CERAMIC-ALL PORCELAIN BRIDGES is EIH.

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Related Devices (Code: EIH)

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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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