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FDA 510(k)

OMRON TRAVEL TOOTHBRUSH/PLAQUE REMOVER #HT-B005

K-Number: K926247 · 1993-04-14

ApplicantOmron Healthcare, Inc.
Decision Date1993-04-14
Product CodeJEQ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

OMRON TRAVEL TOOTHBRUSH/PLAQUE REMOVER #HT-B005 is the device name listed in this FDA 510(k) record. The listed applicant is Omron Healthcare, Inc.. It received FDA 510(k) clearance on 1993-04-14 under 510(k) number K926247. 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 OMRON TRAVEL TOOTHBRUSH/PLAQUE REMOVER #HT-B005?

OMRON TRAVEL TOOTHBRUSH/PLAQUE REMOVER #HT-B005 is a medical device that received FDA 510(k) clearance on 1993-04-14. The listed applicant is Omron Healthcare, Inc.. The 510(k) number is K926247.

When did OMRON TRAVEL TOOTHBRUSH/PLAQUE REMOVER #HT-B005 receive FDA 510(k) clearance?

OMRON TRAVEL TOOTHBRUSH/PLAQUE REMOVER #HT-B005 received FDA 510(k) clearance on 1993-04-14, under 510(k) number K926247.

Who is the listed applicant for OMRON TRAVEL TOOTHBRUSH/PLAQUE REMOVER #HT-B005?

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

What is the FDA product code for OMRON TRAVEL TOOTHBRUSH/PLAQUE REMOVER #HT-B005?

The FDA product code for OMRON TRAVEL TOOTHBRUSH/PLAQUE REMOVER #HT-B005 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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