FDA 510(k) Application Details - K233660

Device Classification Name	System, Image Processing, Radiological   More FDA Info for this Device
510(K) Number	K233660
Device Name	System, Image Processing, Radiological
Applicant	Ionic Health Estrada Dr. Altino Bondensan, 500, Sala 1103 EugΩnio de Melo Sπo JosΘ dos Campos/SP 12247-016 BR Other 510(k) Applications for this Company
Contact	Jose Leovigildo de Melo Coelho Filho 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	11/15/2023
Decision Date	03/18/2024
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