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FDA 510(k)

ADVANCED DENTURE SYSTEM

K-Number: K780722 · 1978-05-26

ApplicantAdvanced Marketing Research Co.
Decision Date1978-05-26
Product CodeEKO
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ADVANCED DENTURE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Marketing Research Co.. It received FDA 510(k) clearance on 1978-05-26 under 510(k) number K780722. The device is classified under product code EKO. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADVANCED DENTURE SYSTEM?

ADVANCED DENTURE SYSTEM is a medical device that received FDA 510(k) clearance on 1978-05-26. The listed applicant is Advanced Marketing Research Co.. The 510(k) number is K780722.

When did ADVANCED DENTURE SYSTEM receive FDA 510(k) clearance?

ADVANCED DENTURE SYSTEM received FDA 510(k) clearance on 1978-05-26, under 510(k) number K780722.

Who is the listed applicant for ADVANCED DENTURE SYSTEM?

The FDA 510(k) record lists Advanced Marketing Research Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ADVANCED DENTURE SYSTEM?

The FDA product code for ADVANCED DENTURE SYSTEM is EKO.

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Related Devices (Code: EKO)

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.

K903672DENE BRIDGEDirotian Pty. , Ltd.K892255DENTAL ROOT ELEVATORZinnanti Surgical Instruments, Inc.K760768FLEXIDENT DENTUREFlexodent Corp.

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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