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FDA 510(k)

SONEX ULTRASONIC TOOTH BRUSH

K-Number: K913724 · 1992-12-28

Decision Date1992-12-28
Product CodeJEQ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SONEX ULTRASONIC TOOTH BRUSH is the device name listed in this FDA 510(k) record. The listed applicant is Sonex Intl., Corp.. It received FDA 510(k) clearance on 1992-12-28 under 510(k) number K913724. 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 SONEX ULTRASONIC TOOTH BRUSH?

SONEX ULTRASONIC TOOTH BRUSH is a medical device that received FDA 510(k) clearance on 1992-12-28. The listed applicant is Sonex Intl., Corp.. The 510(k) number is K913724.

When did SONEX ULTRASONIC TOOTH BRUSH receive FDA 510(k) clearance?

SONEX ULTRASONIC TOOTH BRUSH received FDA 510(k) clearance on 1992-12-28, under 510(k) number K913724.

Who is the listed applicant for SONEX ULTRASONIC TOOTH BRUSH?

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

What is the FDA product code for SONEX ULTRASONIC TOOTH BRUSH?

The FDA product code for SONEX ULTRASONIC 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.

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

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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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