510(k) K000290

LAZERSMILE, LAZERWHITE by Biolase Technology, Inc. — Product Code EFW

K000290 is an FDA 510(k) premarket notification submitted by Biolase Technology, Inc. for the device "LAZERSMILE, LAZERWHITE". The FDA issued a decision of Substantially Equivalent on April 14, 2000. The device falls under product code EFW (Toothbrush, Manual), a Class I device regulated under 21 CFR 872.6855. Biolase Technology, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 14, 2000
Date Received
January 31, 2000
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Toothbrush, Manual
Device Class
Class I
Regulation Number
872.6855
Review Panel
DE
Submission Type