510(k) K935150

SONIPLAK by American Dentronics, Inc. — Product Code JEQ

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