FDA 510(k) Application Details - K243012

Device Classification Name	System, Image Processing, Radiological   More FDA Info for this Device
510(K) Number	K243012
Device Name	System, Image Processing, Radiological
Applicant	MIM Software Inc. 25800 Science Park Drive Suite 180 Cleveland, OH 44122 US Other 510(k) Applications for this Company
Contact	Sydney Lindner Other 510(k) Applications for this Contact
Regulation Number	892.2050   More FDA Info for this Regulation Number
Classification Product Code	LLZ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/27/2024
Decision Date	10/23/2024
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	RA - Radiology
Review Advisory Committee	RA - Radiology
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review