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FDA 510(k)

THE WOOG AND THE WOOG D. POWERED TOOTHBRUSHES

K-Number: K862224 · 1986-09-26

ApplicantXouth, Inc.
Decision Date1986-09-26
Product CodeJEQ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

THE WOOG AND THE WOOG D. POWERED TOOTHBRUSHES is the device name listed in this FDA 510(k) record. The listed applicant is Xouth, Inc.. It received FDA 510(k) clearance on 1986-09-26 under 510(k) number K862224. 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 THE WOOG AND THE WOOG D. POWERED TOOTHBRUSHES?

THE WOOG AND THE WOOG D. POWERED TOOTHBRUSHES is a medical device that received FDA 510(k) clearance on 1986-09-26. The listed applicant is Xouth, Inc.. The 510(k) number is K862224.

When did THE WOOG AND THE WOOG D. POWERED TOOTHBRUSHES receive FDA 510(k) clearance?

THE WOOG AND THE WOOG D. POWERED TOOTHBRUSHES received FDA 510(k) clearance on 1986-09-26, under 510(k) number K862224.

Who is the listed applicant for THE WOOG AND THE WOOG D. POWERED TOOTHBRUSHES?

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

What is the FDA product code for THE WOOG AND THE WOOG D. POWERED TOOTHBRUSHES?

The FDA product code for THE WOOG AND THE WOOG D. POWERED TOOTHBRUSHES is JEQ.

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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.

K200881Oral-B iO Test Drive Power Brush Trial Program KitThe Procter & Gamble CompanyK061351ORAL-B SONIC COMPLETEBraun GmbHK061199ORAL B PROFESSIONALCARE SERIES, ORAL B ADVANCEPOWER SERIESBraun GmbHK040416SONICARE ADVANCE TOOTHBRUSH, MODEL 4900Philips Oral Healthcare, Inc.K022900BUTLER GUM VARI-CLEAN POWER TOOTHBRUSHESJohn O. Butler Co.K012914SONICWAVE SONIC PLAQUE REMOVERHomedics, Inc.

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.

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