FDA 510(k) Application Details - K241364

Device Classification Name	System, Tomography, Computed, Emission   More FDA Info for this Device
510(K) Number	K241364
Device Name	System, Tomography, Computed, Emission
Applicant	Hermes Medical Solutions AB Strandbergsgatan 16 Stockholm 11251 SE Other 510(k) Applications for this Company
Contact	Hanne Grinaker Other 510(k) Applications for this Contact
Regulation Number	892.1200   More FDA Info for this Regulation Number
Classification Product Code	KPS Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/14/2024
Decision Date	11/08/2024
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	RA - Radiology
Review Advisory Committee	RA - Radiology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review