ORAL B PROFESSIONALCARE SERIES, ORAL B ADVANCEPOWER SERIES
K-Number: K061199 · 2006-05-31
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Device Summary
Frequently Asked Questions
What is the ORAL B PROFESSIONALCARE SERIES, ORAL B ADVANCEPOWER SERIES?
ORAL B PROFESSIONALCARE SERIES, ORAL B ADVANCEPOWER SERIES is a medical device that received FDA 510(k) clearance on 2006-05-31. The listed applicant is Braun GmbH. The 510(k) number is K061199.
When did ORAL B PROFESSIONALCARE SERIES, ORAL B ADVANCEPOWER SERIES receive FDA 510(k) clearance?
ORAL B PROFESSIONALCARE SERIES, ORAL B ADVANCEPOWER SERIES received FDA 510(k) clearance on 2006-05-31, under 510(k) number K061199.
Who is the listed applicant for ORAL B PROFESSIONALCARE SERIES, ORAL B ADVANCEPOWER SERIES?
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 PROFESSIONALCARE SERIES, ORAL B ADVANCEPOWER SERIES?
The FDA product code for ORAL B PROFESSIONALCARE SERIES, ORAL B ADVANCEPOWER SERIES is JEQ.
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.
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.
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.
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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