FDA 510(k) Application Details - K242301

Device Classification Name	More FDA Info for this Device
510(K) Number	K242301
Device Name	Socrates 38 Catheter
Applicant	Scientia Vascular Inc 2460 South 3270 West West Valley City, UT 84119 US Other 510(k) Applications for this Company
Contact	Thomas Lippert Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	QJP Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/02/2024
Decision Date	12/04/2024
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	NE - Neurology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review