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FDA 510(k)

DENTURE ADJUSTMENT KIT

K-Number: K820685 · 1982-04-09

Decision Date1982-04-09
Product CodeEBO
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DENTURE ADJUSTMENT KIT is the device name listed in this FDA 510(k) record. The listed applicant is Camdent Laboratories. It received FDA 510(k) clearance on 1982-04-09 under 510(k) number K820685. The device is classified under product code EBO. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DENTURE ADJUSTMENT KIT?

DENTURE ADJUSTMENT KIT is a medical device that received FDA 510(k) clearance on 1982-04-09. The listed applicant is Camdent Laboratories. The 510(k) number is K820685.

When did DENTURE ADJUSTMENT KIT receive FDA 510(k) clearance?

DENTURE ADJUSTMENT KIT received FDA 510(k) clearance on 1982-04-09, under 510(k) number K820685.

Who is the listed applicant for DENTURE ADJUSTMENT KIT?

The FDA 510(k) record lists Camdent Laboratories as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DENTURE ADJUSTMENT KIT?

The FDA product code for DENTURE ADJUSTMENT KIT is EBO.

Related Clinical Trials

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.

Related Devices (Code: EBO)

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.

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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