FDA 510(k) Applications for Medical Device Product Code: PBK ()

FDA 510(k) Applications for Medical Device Product Code "PBK"

FDA 510(k) Number	Applicant	Device Name	Decision Date
K221834	Centers For Disease Control And Prevention	Non-variola Orthopoxvirus Real-time PCR Primer and Probe Set	06/24/2022
DEN070001	CENTERS FOR DISEASE CONTROL AND PREVENTION	NON-VARIOLA ORTHOPOXVIRUS REAL-TIME PCR PRIMER AND PROBE SET	09/21/2018
K181205	Centers for Disease Control and Prevention	Non-variola Orthopoxvirus Real-time PCR Primer and Probe Set	09/20/2018
K222558	Centers for Disease Control and Prevention	Non-variola Orthopoxvirus Real-time PCR Primer and Probe Set	08/30/2022
K221658	Centers for Disease Control and Prevention	Non-variola Orthopoxvirus Real-time PCR Primer and Probe Set	06/10/2022