OPTEX BLOOD GAS MONITORING SYSTEM
Jan 1990
63d
Optex Biomedical
1
Total
1
Cleared
0
Denied
Optex Biomedical — FDA 510(k) Submissions
Optex Biomedical has submitted 1 FDA 510(k) premarket notifications since 1990, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Analyzer, Gas, Oxygen, Partial Pressure, Blood-phase, Indwelling . Use the specialty filter in the sidebar to narrow results.
1 devices