FDA 510(k) Application Details - K201489

Device Classification Name	Introducer, Catheter   More FDA Info for this Device
510(K) Number	K201489
Device Name	Introducer, Catheter
Applicant	Argon Medical Devices, Inc. 1445 Flat Creek Road Athens, TX 75751 US Other 510(k) Applications for this Company
Contact	Amy Clendening-Wheeler Other 510(k) Applications for this Contact
Regulation Number	870.1340   More FDA Info for this Regulation Number
Classification Product Code	DYB Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/04/2020
Decision Date	12/22/2020
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