FDA 510(k)

DUO DENT

K-Number: K923694 · 1994-05-18

Decision Date1994-05-18

Product CodeDZE

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

DUO DENT is the device name listed in this FDA 510(k) record. The listed applicant is Pdc Management Services, Inc.. It received FDA 510(k) clearance on 1994-05-18 under 510(k) number K923694. The device is classified under product code DZE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DUO DENT?

DUO DENT is a medical device that received FDA 510(k) clearance on 1994-05-18. The listed applicant is Pdc Management Services, Inc.. The 510(k) number is K923694.

When did DUO DENT receive FDA 510(k) clearance?

DUO DENT received FDA 510(k) clearance on 1994-05-18, under 510(k) number K923694.

Who is the listed applicant for DUO DENT?

The FDA 510(k) record lists Pdc Management Services, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DUO DENT?

The FDA product code for DUO DENT is DZE.

Related Devices (Code: DZE)

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.