Procise CRP, ProciseDx Analyzer, ProciseDx Calibration Cartridge
Nov 2022
907d
Procise Diagnostics
1
Total
1
Cleared
0
Denied
Procise Diagnostics — FDA 510(k) Submissions
Procise Diagnostics has submitted 1 FDA 510(k) premarket notifications since 2022, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include C-reactive Protein, Antigen, Antiserum, And Control . Use the specialty filter in the sidebar to narrow results.
1 devices