Janssen Pharmaceutica NV is one of 40 FDA 510(k) medical device manufacturers from Belgium in the dataset, ranked by real submission volume.
Janssen Pharmaceutica NV - FDA 510(k) Cleared Devices
Recent clearances: Idylla Respiratory (IFV-RSV) Panel
1
Total
1
Cleared
0
Denied
Janssen Pharmaceutica NV has 1 FDA 510(k) cleared medical devices. Based in Beerse, BE.
Historical record: 1 cleared submissions from 2017 to 2017. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Janssen Pharmaceutica NV Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Janssen Research & Development, LLC as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Janssen Pharmaceutica NV
1 devices