FDA 510(k) Application Details - K182699

Device Classification Name	Catheters, Transluminal Coronary Angioplasty, Percutaneous   More FDA Info for this Device
510(K) Number	K182699
Device Name	Catheters, Transluminal Coronary Angioplasty, Percutaneous
Applicant	Kossel Medtech (Suzhou) Co., Ltd. F3, BLDG 6, No. 8, Jinfeng Road Suzhou 215163 CN Other 510(k) Applications for this Company
Contact	Zane Wang Other 510(k) Applications for this Contact
Regulation Number	000.0000   More FDA Info for this Regulation Number
Classification Product Code	LOX Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/27/2018
Decision Date	11/26/2018
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