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FDA 510(k)

PARTIAL DENTURE ALLOY

K-Number: K833512 · 1983-12-27

ApplicantDentsply Intl.
Decision Date1983-12-27
Product CodeEJH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PARTIAL DENTURE ALLOY is the device name listed in this FDA 510(k) record. The listed applicant is Dentsply Intl.. It received FDA 510(k) clearance on 1983-12-27 under 510(k) number K833512. The device is classified under product code EJH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PARTIAL DENTURE ALLOY?

PARTIAL DENTURE ALLOY is a medical device that received FDA 510(k) clearance on 1983-12-27. The listed applicant is Dentsply Intl.. The 510(k) number is K833512.

When did PARTIAL DENTURE ALLOY receive FDA 510(k) clearance?

PARTIAL DENTURE ALLOY received FDA 510(k) clearance on 1983-12-27, under 510(k) number K833512.

Who is the listed applicant for PARTIAL DENTURE ALLOY?

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 PARTIAL DENTURE ALLOY?

The FDA product code for PARTIAL DENTURE ALLOY is EJH.

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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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