FDA 510(k) Application Details - K240384

Device Classification Name	Catheter, Percutaneous   More FDA Info for this Device
510(K) Number	K240384
Device Name	Catheter, Percutaneous
Applicant	Okami Medical, Inc. 8 Argonaut, Suite 100 Aliso Viejo, CA 92656 US Other 510(k) Applications for this Company
Contact	Jill Delsman Other 510(k) Applications for this Contact
Regulation Number	870.1250   More FDA Info for this Regulation Number
Classification Product Code	DQY Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/08/2024
Decision Date	03/08/2024
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