FDA 510(k) Application Details - K251103

Device Classification Name	Catheter, Ultrasound, Intravascular   More FDA Info for this Device
510(K) Number	K251103
Device Name	Catheter, Ultrasound, Intravascular
Applicant	Philips Image Guided Therapy Corporation 3721 Valley Centre Drive Suite 500 San Diego, CA 92130 US Other 510(k) Applications for this Company
Contact	Travis Pittman Other 510(k) Applications for this Contact
Regulation Number	870.1200   More FDA Info for this Regulation Number
Classification Product Code	OBJ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/11/2025
Decision Date	05/09/2025
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review