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FDA 510(k)

SONICARE ADVANCE TOOTHBRUSH, MODEL 4900

K-Number: K040416 · 2004-07-02

ApplicantPhilips Oral Healthcare, Inc.
Decision Date2004-07-02
Product CodeJEQ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SONICARE ADVANCE TOOTHBRUSH, MODEL 4900 is the device name listed in this FDA 510(k) record. The listed applicant is Philips Oral Healthcare, Inc.. It received FDA 510(k) clearance on 2004-07-02 under 510(k) number K040416. 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 SONICARE ADVANCE TOOTHBRUSH, MODEL 4900?

SONICARE ADVANCE TOOTHBRUSH, MODEL 4900 is a medical device that received FDA 510(k) clearance on 2004-07-02. The listed applicant is Philips Oral Healthcare, Inc.. The 510(k) number is K040416.

When did SONICARE ADVANCE TOOTHBRUSH, MODEL 4900 receive FDA 510(k) clearance?

SONICARE ADVANCE TOOTHBRUSH, MODEL 4900 received FDA 510(k) clearance on 2004-07-02, under 510(k) number K040416.

Who is the listed applicant for SONICARE ADVANCE TOOTHBRUSH, MODEL 4900?

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

What is the FDA product code for SONICARE ADVANCE TOOTHBRUSH, MODEL 4900?

The FDA product code for SONICARE ADVANCE TOOTHBRUSH, MODEL 4900 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 GmbHK022900BUTLER 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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