FDA 510(k) Application Details - K241280

Device Classification Name	More FDA Info for this Device
510(K) Number	K241280
Device Name	Constellation (CON-001)
Applicant	Q Bio, Inc. 1411 Industrial Road San Carlos, CA 94070 US Other 510(k) Applications for this Company
Contact	Clarissa Shen 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	05/07/2024
Decision Date	09/12/2024
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