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FDA 510(k)

THE WOOG ORABRUSH

K-Number: K871406 · 1987-07-07

ApplicantWoog Intl.
Decision Date1987-07-07
Product CodeJEQ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

THE WOOG ORABRUSH is the device name listed in this FDA 510(k) record. The listed applicant is Woog Intl.. It received FDA 510(k) clearance on 1987-07-07 under 510(k) number K871406. 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 ORABRUSH?

THE WOOG ORABRUSH is a medical device that received FDA 510(k) clearance on 1987-07-07. The listed applicant is Woog Intl.. The 510(k) number is K871406.

When did THE WOOG ORABRUSH receive FDA 510(k) clearance?

THE WOOG ORABRUSH received FDA 510(k) clearance on 1987-07-07, under 510(k) number K871406.

Who is the listed applicant for THE WOOG ORABRUSH?

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

What is the FDA product code for THE WOOG ORABRUSH?

The FDA product code for THE WOOG ORABRUSH 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Woog Intl. 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.

K874374THE WOOG ORATEST

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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