FDA 510(k) Application Details - K233117

Device Classification Name	Controller, Foot, Handpiece And Cord   More FDA Info for this Device
510(K) Number	K233117
Device Name	Controller, Foot, Handpiece And Cord
Applicant	Nakanishi Inc. 700 Shimohinata Kanuma 322-8666 JP Other 510(k) Applications for this Company
Contact	Masaaki Kikuchi Other 510(k) Applications for this Contact
Regulation Number	872.4200   More FDA Info for this Regulation Number
Classification Product Code	EBW Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/27/2023
Decision Date	06/20/2024
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