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)

PLAK TRAC POWERED TOOTHBRUSH

K-Number: K896245 · 1990-03-28

Decision Date1990-03-28
Product CodeJEQ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PLAK TRAC POWERED TOOTHBRUSH is the device name listed in this FDA 510(k) record. The listed applicant is Windmere Corp.. It received FDA 510(k) clearance on 1990-03-28 under 510(k) number K896245. The device is classified under product code JEQ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PLAK TRAC POWERED TOOTHBRUSH?

PLAK TRAC POWERED TOOTHBRUSH is a medical device that received FDA 510(k) clearance on 1990-03-28. The listed applicant is Windmere Corp.. The 510(k) number is K896245.

When did PLAK TRAC POWERED TOOTHBRUSH receive FDA 510(k) clearance?

PLAK TRAC POWERED TOOTHBRUSH received FDA 510(k) clearance on 1990-03-28, under 510(k) number K896245.

Who is the listed applicant for PLAK TRAC POWERED TOOTHBRUSH?

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

What is the FDA product code for PLAK TRAC POWERED TOOTHBRUSH?

The FDA product code for PLAK TRAC POWERED TOOTHBRUSH is JEQ.

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 Windmere Corp. 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.

View all 7 devices →

Related Devices (Code: JEQ)

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.

↑