FDA 510(k) Application Details - K233904

Device Classification Name	Transducer, Pressure, Catheter Tip   More FDA Info for this Device
510(K) Number	K233904
Device Name	Transducer, Pressure, Catheter Tip
Applicant	Acist Medical Systems, Inc 7905 Fuller Rd Eden Prairie, MN 55344 US Other 510(k) Applications for this Company
Contact	Bobbie Daughters Other 510(k) Applications for this Contact
Regulation Number	870.2870   More FDA Info for this Regulation Number
Classification Product Code	DXO Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/11/2023
Decision Date	07/17/2024
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