ORAL-B SUB-BRAND MANUAL TOOTHBRUSH
K-Number: K073224 · 2008-02-06
Advertisement
Device Summary
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.
Advertisement