510(k) K061199
K061199 is an FDA 510(k) premarket notification submitted by Braun GmbH for the device "ORAL B PROFESSIONALCARE SERIES, ORAL B ADVANCEPOWER SERIES". The FDA issued a decision of Substantially Equivalent on May 31, 2006. The device falls under product code JEQ (Toothbrush, Powered), a Class I device regulated under 21 CFR 872.6865. Braun GmbH has at least 8 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 31, 2006
- Date Received
- April 28, 2006
- 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