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)

ELECTRIC TOOTH-BRUSH

K-Number: K931360 · 1993-07-13

Decision Date1993-07-13
Product CodeJEQ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ELECTRIC TOOTH-BRUSH is the device name listed in this FDA 510(k) record. The listed applicant is U.S. Dentek Corp.. It received FDA 510(k) clearance on 1993-07-13 under 510(k) number K931360. 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 ELECTRIC TOOTH-BRUSH?

ELECTRIC TOOTH-BRUSH is a medical device that received FDA 510(k) clearance on 1993-07-13. The listed applicant is U.S. Dentek Corp.. The 510(k) number is K931360.

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

ELECTRIC TOOTH-BRUSH received FDA 510(k) clearance on 1993-07-13, under 510(k) number K931360.

Who is the listed applicant for ELECTRIC TOOTH-BRUSH?

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

What is the FDA product code for ELECTRIC TOOTH-BRUSH?

The FDA product code for ELECTRIC TOOTH-BRUSH 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 U.S. Dentek 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.

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.

↑