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FDA 510(k)

DICOR CERAMIC INLAY - NEW TECHNIC

K-Number: K884166 · 1989-04-17

ApplicantDentsply Intl.
Decision Date1989-04-17
Product CodeELW
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DICOR CERAMIC INLAY - NEW TECHNIC is the device name listed in this FDA 510(k) record. The listed applicant is Dentsply Intl.. It received FDA 510(k) clearance on 1989-04-17 under 510(k) number K884166. The device is classified under product code ELW. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DICOR CERAMIC INLAY - NEW TECHNIC?

DICOR CERAMIC INLAY - NEW TECHNIC is a medical device that received FDA 510(k) clearance on 1989-04-17. The listed applicant is Dentsply Intl.. The 510(k) number is K884166.

When did DICOR CERAMIC INLAY - NEW TECHNIC receive FDA 510(k) clearance?

DICOR CERAMIC INLAY - NEW TECHNIC received FDA 510(k) clearance on 1989-04-17, under 510(k) number K884166.

Who is the listed applicant for DICOR CERAMIC INLAY - NEW TECHNIC?

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 CERAMIC INLAY - NEW TECHNIC?

The FDA product code for DICOR CERAMIC INLAY - NEW TECHNIC is ELW.

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Related Devices (Code: ELW)

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.

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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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