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FDA 510(k)

TX ELECTRIC TOOTHBRUSH

K-Number: K921773 · 1992-07-13

ApplicantOptiva Corp.
Decision Date1992-07-13
Product CodeJEQ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

TX ELECTRIC TOOTHBRUSH is the device name listed in this FDA 510(k) record. The listed applicant is Optiva Corp.. It received FDA 510(k) clearance on 1992-07-13 under 510(k) number K921773. 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 TX ELECTRIC TOOTHBRUSH?

TX ELECTRIC TOOTHBRUSH is a medical device that received FDA 510(k) clearance on 1992-07-13. The listed applicant is Optiva Corp.. The 510(k) number is K921773.

When did TX ELECTRIC TOOTHBRUSH receive FDA 510(k) clearance?

TX ELECTRIC TOOTHBRUSH received FDA 510(k) clearance on 1992-07-13, under 510(k) number K921773.

Who is the listed applicant for TX ELECTRIC TOOTHBRUSH?

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

What is the FDA product code for TX ELECTRIC TOOTHBRUSH?

The FDA product code for TX ELECTRIC TOOTHBRUSH 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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