Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

DENTURE CLEANSER & TOOTHPASTE IN ONE

K-Number: K780254 · 1978-03-09

Decision Date1978-03-09
Product CodeJER
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DENTURE CLEANSER & TOOTHPASTE IN ONE is the device name listed in this FDA 510(k) record. The listed applicant is Richardson Merrel, Inc.. It received FDA 510(k) clearance on 1978-03-09 under 510(k) number K780254. The device is classified under product code JER. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DENTURE CLEANSER & TOOTHPASTE IN ONE?

DENTURE CLEANSER & TOOTHPASTE IN ONE is a medical device that received FDA 510(k) clearance on 1978-03-09. The listed applicant is Richardson Merrel, Inc.. The 510(k) number is K780254.

When did DENTURE CLEANSER & TOOTHPASTE IN ONE receive FDA 510(k) clearance?

DENTURE CLEANSER & TOOTHPASTE IN ONE received FDA 510(k) clearance on 1978-03-09, under 510(k) number K780254.

Who is the listed applicant for DENTURE CLEANSER & TOOTHPASTE IN ONE?

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

What is the FDA product code for DENTURE CLEANSER & TOOTHPASTE IN ONE?

The FDA product code for DENTURE CLEANSER & TOOTHPASTE IN ONE is JER.

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 Richardson Merrel, 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.

Related Devices (Code: JER)

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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑