510(k) K200881
K200881 is an FDA 510(k) premarket notification submitted by The Procter & Gamble Company for the device "Oral-B iO Test Drive Power Brush Trial Program Kit". The FDA issued a decision of Substantially Equivalent on August 27, 2020. The device falls under product code JEQ (Toothbrush, Powered), a Class I device regulated under 21 CFR 872.6865. The Procter & Gamble Company has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 27, 2020
- Date Received
- April 2, 2020
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Toothbrush, Powered
- Device Class
- Class I
- Regulation Number
- 872.6865
- Review Panel
- DE
- Submission Type