510(k) K935150
K935150 is an FDA 510(k) premarket notification submitted by American Dentronics, Inc. for the device "SONIPLAK". The FDA issued a decision of Substantially Equivalent on May 18, 1994. The device falls under product code JEQ (Toothbrush, Powered), a Class I device regulated under 21 CFR 872.6865. American Dentronics, Inc. has at least 3 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 18, 1994
- Date Received
- October 28, 1993
- 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