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FDA 510(k)

MY BEAT POWERED TOOTHBRUSH

K-Number: K941209 · 1994-06-16

Decision Date1994-06-16
Product CodeJEQ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MY BEAT POWERED TOOTHBRUSH is the device name listed in this FDA 510(k) record. The listed applicant is Sanwa Components USA, Inc.. It received FDA 510(k) clearance on 1994-06-16 under 510(k) number K941209. 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 MY BEAT POWERED TOOTHBRUSH?

MY BEAT POWERED TOOTHBRUSH is a medical device that received FDA 510(k) clearance on 1994-06-16. The listed applicant is Sanwa Components USA, Inc.. The 510(k) number is K941209.

When did MY BEAT POWERED TOOTHBRUSH receive FDA 510(k) clearance?

MY BEAT POWERED TOOTHBRUSH received FDA 510(k) clearance on 1994-06-16, under 510(k) number K941209.

Who is the listed applicant for MY BEAT POWERED TOOTHBRUSH?

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

What is the FDA product code for MY BEAT POWERED TOOTHBRUSH?

The FDA product code for MY BEAT 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.

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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