FDA 510(k) Application Details - K232174

Device Classification Name	Powder, Porcelain   More FDA Info for this Device
510(K) Number	K232174
Device Name	Powder, Porcelain
Applicant	Genoss Co., Ltd. 1F, 106, Jeongoksandan-ro, Seosin-myeon Hwaseong-si 16229 KR Other 510(k) Applications for this Company
Contact	Hayoung Sung Other 510(k) Applications for this Contact
Regulation Number	872.6660   More FDA Info for this Regulation Number
Classification Product Code	EIH Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/21/2023
Decision Date	02/23/2024
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