Oral-B iO Test Drive Power Brush Trial Program Kit
K-Number: K200881 · 2020-08-27
ApplicantThe Procter & Gamble Company
Decision Date2020-08-27
Product CodeJEQ
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
Oral-B iO Test Drive Power Brush Trial Program Kit is a medical device manufactured by The Procter & Gamble Company. It received FDA 510(k) clearance on 2020-08-27 under approval number K200881. 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 iO Test Drive Power Brush Trial Program Kit?
Oral-B iO Test Drive Power Brush Trial Program Kit is a medical device that received FDA 510(k) clearance on 2020-08-27. It is manufactured by The Procter & Gamble Company. The 510(k) number is K200881.
When was Oral-B iO Test Drive Power Brush Trial Program Kit approved by the FDA?
Oral-B iO Test Drive Power Brush Trial Program Kit received FDA 510(k) clearance on 2020-08-27, under approval number K200881.
What company makes Oral-B iO Test Drive Power Brush Trial Program Kit?
Oral-B iO Test Drive Power Brush Trial Program Kit is manufactured by The Procter & Gamble Company.
What is the FDA product code for Oral-B iO Test Drive Power Brush Trial Program Kit?
The FDA product code for Oral-B iO Test Drive Power Brush Trial Program Kit is JEQ.
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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.