FDA 510(k) Application Details - K242776

Device Classification Name	Device, Percutaneous Retrieval   More FDA Info for this Device
510(K) Number	K242776
Device Name	Device, Percutaneous Retrieval
Applicant	LimFlow Inc. 6001 Oak Canyon Suite 100 Irvine, CA 92618 US Other 510(k) Applications for this Company
Contact	Tosan Eweka Other 510(k) Applications for this Contact
Regulation Number	870.5150   More FDA Info for this Regulation Number
Classification Product Code	MMX Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/13/2024
Decision Date	02/14/2025
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