FDA 510(k) Application Details - K251096

Device Classification Name	More FDA Info for this Device
510(K) Number	K251096
Device Name	PeekMed web
Applicant	Peek Health, S.A. Centro de Neg≤cios Ideia AtlΓntico, Rua Padres Carmelitas Braga 4719-005 PT Other 510(k) Applications for this Company
Contact	Sara Silva Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	QIH Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/10/2025
Decision Date	07/14/2025
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