FDA 510(k) Application Details - K121901

Device Classification Name	Handpiece, Contra- And Right-Angle Attachment, Dental   More FDA Info for this Device
510(K) Number	K121901
Device Name	Handpiece, Contra- And Right-Angle Attachment, Dental
Applicant	NAKANISHI, INC. 4-4-17 HONGO BUNKYO-KU 113-0033 JP Other 510(k) Applications for this Company
Contact	FUMIAKI KANAI Other 510(k) Applications for this Contact
Regulation Number	872.4200   More FDA Info for this Regulation Number
Classification Product Code	EGS Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/29/2012
Decision Date	02/28/2013
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	DE - Dental
Review Advisory Committee	DE - Dental
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review