FDA 510(k) Application Details - K241851

Device Classification Name	More FDA Info for this Device
510(K) Number	K241851
Device Name	VersusÖ Catheter (VS110-8B)
Applicant	Liquet Medical Inc. 5619 Country Hills Ln Glen Allen, VA 23059 US Other 510(k) Applications for this Company
Contact	John Schindler Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	QEY Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/27/2024
Decision Date	11/25/2024
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