FDA 510(k) Application Details - K241158

Device Classification Name	Catheter, Percutaneous   More FDA Info for this Device
510(K) Number	K241158
Device Name	Catheter, Percutaneous
Applicant	Asahi Intecc Co., Ltd. 3-100 Akatsuki-cho Seto 489-0071 JP Other 510(k) Applications for this Company
Contact	Fujimura Katsuhiko Other 510(k) Applications for this Contact
Regulation Number	870.1250   More FDA Info for this Regulation Number
Classification Product Code	DQY Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/26/2024
Decision Date	06/25/2024
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review