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)

TOTE-BRUSH

K-Number: K800154 · 1980-02-05

Decision Date1980-02-05
Product CodeEFW
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

TOTE-BRUSH is the device name listed in this FDA 510(k) record. The listed applicant is Anja Marketing, Inc.. It received FDA 510(k) clearance on 1980-02-05 under 510(k) number K800154. The device is classified under product code EFW. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TOTE-BRUSH?

TOTE-BRUSH is a medical device that received FDA 510(k) clearance on 1980-02-05. The listed applicant is Anja Marketing, Inc.. The 510(k) number is K800154.

When did TOTE-BRUSH receive FDA 510(k) clearance?

TOTE-BRUSH received FDA 510(k) clearance on 1980-02-05, under 510(k) number K800154.

Who is the listed applicant for TOTE-BRUSH?

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

What is the FDA product code for TOTE-BRUSH?

The FDA product code for TOTE-BRUSH is EFW.

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: EFW)

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.

↑