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FDA 510(k)

ORAL-B SONIC COMPLETE

K-Number: K061351 · 2006-06-05

ApplicantBraun GmbH
Decision Date2006-06-05
Product CodeJEQ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ORAL-B SONIC COMPLETE is the device name listed in this FDA 510(k) record. The listed applicant is Braun GmbH. It received FDA 510(k) clearance on 2006-06-05 under 510(k) number K061351. 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 ORAL-B SONIC COMPLETE?

ORAL-B SONIC COMPLETE is a medical device that received FDA 510(k) clearance on 2006-06-05. The listed applicant is Braun GmbH. The 510(k) number is K061351.

When did ORAL-B SONIC COMPLETE receive FDA 510(k) clearance?

ORAL-B SONIC COMPLETE received FDA 510(k) clearance on 2006-06-05, under 510(k) number K061351.

Who is the listed applicant for ORAL-B SONIC COMPLETE?

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

What is the FDA product code for ORAL-B SONIC COMPLETE?

The FDA product code for ORAL-B SONIC COMPLETE is JEQ.

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Other records listing Braun GmbH 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.

K061199ORAL B PROFESSIONALCARE SERIES, ORAL B ADVANCEPOWER SERIESK060006BRAUN THERMOSCAN IRT 2000 INFRARED EAR THERMOMETERK031928BRAUN THERMOSCAN PRO 4000 SERIES (PROFESSIONAL USE ENVIRONMENT); BRAUN THERMOSCAN IRT 4000 SERIES (HOME USE ENVIRONMENT)K012035BRAUN PRECISION SENSOR PRO, MODEL BP 2590K003732BRAUN PRECISION SENSOR, MODEL BP 2000 SERIESK992468BRAUN THERMOSCAN PRO3000 INFARED THERMOMETER

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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 CompanyK061199ORAL 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.K970381POWERED TOOTHBRUSHEmjoi Action USA, Ltd.

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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