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FDA 510(k)

DENTROL LIQUID DENTURE ADHESIVE

K-Number: K780849 · 1978-07-31

Decision Date1978-07-31
Product Code
DecisionSubstantially Equivalent

Device Summary

DENTROL LIQUID DENTURE ADHESIVE is the device name listed in this FDA 510(k) record. The listed applicant is Block Drug Company, Inc.. It received FDA 510(k) clearance on 1978-07-31 under 510(k) number K780849. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DENTROL LIQUID DENTURE ADHESIVE?

DENTROL LIQUID DENTURE ADHESIVE is a medical device that received FDA 510(k) clearance on 1978-07-31. The listed applicant is Block Drug Company, Inc.. The 510(k) number is K780849.

When did DENTROL LIQUID DENTURE ADHESIVE receive FDA 510(k) clearance?

DENTROL LIQUID DENTURE ADHESIVE received FDA 510(k) clearance on 1978-07-31, under 510(k) number K780849.

Who is the listed applicant for DENTROL LIQUID DENTURE ADHESIVE?

The FDA 510(k) record lists Block Drug Company, Inc. as the applicant. This does not by itself establish the device manufacturer.

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.

Other records listing Block Drug Company, Inc. as applicant

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.

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