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FDA 510(k)

OMRON TRAVEL TOOTHBRUSH, MODEL HT-B02

K-Number: K901963 · 1990-06-26

ApplicantOmron Marshall Products, Inc.
Decision Date1990-06-26
Product CodeJEQ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

OMRON TRAVEL TOOTHBRUSH, MODEL HT-B02 is the device name listed in this FDA 510(k) record. The listed applicant is Omron Marshall Products, Inc.. It received FDA 510(k) clearance on 1990-06-26 under 510(k) number K901963. 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, MODEL HT-B02?

OMRON TRAVEL TOOTHBRUSH, MODEL HT-B02 is a medical device that received FDA 510(k) clearance on 1990-06-26. The listed applicant is Omron Marshall Products, Inc.. The 510(k) number is K901963.

When did OMRON TRAVEL TOOTHBRUSH, MODEL HT-B02 receive FDA 510(k) clearance?

OMRON TRAVEL TOOTHBRUSH, MODEL HT-B02 received FDA 510(k) clearance on 1990-06-26, under 510(k) number K901963.

Who is the listed applicant for OMRON TRAVEL TOOTHBRUSH, MODEL HT-B02?

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

What is the FDA product code for OMRON TRAVEL TOOTHBRUSH, MODEL HT-B02?

The FDA product code for OMRON TRAVEL TOOTHBRUSH, MODEL HT-B02 is JEQ.

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Other records listing Omron Marshall Products, Inc. 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.

K903133OMRON OSCILLOMETRIC DIGITAL BP MONITOR-HEM-405CK903134OMRON AUTO OSCILLOMETRIC DIG BP MONT/HEM-704C 705C

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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