ImmuView S pneumoniae and L pneumophila Urinary Antigen Test
Mar 2020
307d
Ssi Diagnostica A/S
1
Total
1
Cleared
0
Denied
Ssi Diagnostica A/S — FDA 510(k) Submissions
Ssi Diagnostica A/S has submitted 1 FDA 510(k) premarket notifications since 2020, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Legionella, Spp., Elisa . Use the specialty filter in the sidebar to narrow results.
1 devices