FDA 510(k) Application Details - K102871

Device Classification Name	Toothbrush, Manual   More FDA Info for this Device
510(K) Number	K102871
Device Name	Toothbrush, Manual
Applicant	PIAVE SPAZZOLIFICIO S.P.A. 212 W 91ST ST APT 812 NEW YORK, NY 10024 US Other 510(k) Applications for this Company
Contact	KEILA LACOURT Other 510(k) Applications for this Contact
Regulation Number	872.6855   More FDA Info for this Regulation Number
Classification Product Code	EFW Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/30/2010
Decision Date	10/03/2011
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	DE - Dental
Review Advisory Committee	DE - Dental
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review