Ssi Diagnostica A/S is one of 44 FDA 510(k) medical device manufacturers from Denmark in the dataset, ranked by real submission volume.
Ssi Diagnostica A/S - FDA 510(k) Cleared Devices
Recent clearances: ImmuView S pneumoniae and L pneumophila Urinary Antigen Test
1
Total
1
Cleared
0
Denied
Ssi Diagnostica A/S has 1 FDA 510(k) cleared medical devices. Based in Hilleroed, DK.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Ssi Diagnostica A/S Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Bentsen Regulatory and Clinicals Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Ssi Diagnostica A/S
1 devices