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FDA 510(k)

ORAL-B SUB-BRAND MANUAL TOOTHBRUSH

K-Number: K073224 · 2008-02-06

Decision Date2008-02-06
Product CodeEFW
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ORAL-B SUB-BRAND MANUAL TOOTHBRUSH is the device name listed in this FDA 510(k) record. The listed applicant is Procter & Gamble. It received FDA 510(k) clearance on 2008-02-06 under 510(k) number K073224. The device is classified under product code EFW. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ORAL-B SUB-BRAND MANUAL TOOTHBRUSH?

ORAL-B SUB-BRAND MANUAL TOOTHBRUSH is a medical device that received FDA 510(k) clearance on 2008-02-06. The listed applicant is Procter & Gamble. The 510(k) number is K073224.

When did ORAL-B SUB-BRAND MANUAL TOOTHBRUSH receive FDA 510(k) clearance?

ORAL-B SUB-BRAND MANUAL TOOTHBRUSH received FDA 510(k) clearance on 2008-02-06, under 510(k) number K073224.

Who is the listed applicant for ORAL-B SUB-BRAND MANUAL TOOTHBRUSH?

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

What is the FDA product code for ORAL-B SUB-BRAND MANUAL TOOTHBRUSH?

The FDA product code for ORAL-B SUB-BRAND MANUAL TOOTHBRUSH is EFW.

Related Clinical Trials

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.

Related Devices (Code: EFW)

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.

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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