FDA 510(k) Application Details - K242212

Device Classification Name	Injector And Syringe, Angiographic   More FDA Info for this Device
510(K) Number	K242212
Device Name	Injector And Syringe, Angiographic
Applicant	Nemoto Kyorindo Co., Ltd. 2-27-20 Hongo Bunkyo-ku Tokyo 113-0033 JP Other 510(k) Applications for this Company
Contact	Jim Knipfer Other 510(k) Applications for this Contact
Regulation Number	870.1650   More FDA Info for this Regulation Number
Classification Product Code	DXT Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/29/2024
Decision Date	08/27/2024
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	Y
Expedited Review