FDA 510(k) Application Details - K183195

Device Classification Name	Computer, Diagnostic, Programmable   More FDA Info for this Device
510(K) Number	K183195
Device Name	Computer, Diagnostic, Programmable
Applicant	Catheter Precision, Inc. 1705 Route 46 Ledgewood, NJ 07852 US Other 510(k) Applications for this Company
Contact	Steve Adler Other 510(k) Applications for this Contact
Regulation Number	870.1425   More FDA Info for this Regulation Number
Classification Product Code	DQK Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/19/2018
Decision Date	06/14/2019
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