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FDA 510(k)

PORCELAIN POWDER FOR CLINICAL USE

K-Number: K810096 · 1981-03-04

ApplicantDentsply Intl.
Decision Date1981-03-04
Product CodeEIH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PORCELAIN POWDER FOR CLINICAL USE is the device name listed in this FDA 510(k) record. The listed applicant is Dentsply Intl.. It received FDA 510(k) clearance on 1981-03-04 under 510(k) number K810096. 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 PORCELAIN POWDER FOR CLINICAL USE?

PORCELAIN POWDER FOR CLINICAL USE is a medical device that received FDA 510(k) clearance on 1981-03-04. The listed applicant is Dentsply Intl.. The 510(k) number is K810096.

When did PORCELAIN POWDER FOR CLINICAL USE receive FDA 510(k) clearance?

PORCELAIN POWDER FOR CLINICAL USE received FDA 510(k) clearance on 1981-03-04, under 510(k) number K810096.

Who is the listed applicant for PORCELAIN POWDER FOR CLINICAL USE?

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 PORCELAIN POWDER FOR CLINICAL USE?

The FDA product code for PORCELAIN POWDER FOR CLINICAL USE is 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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