Ohmeda Medical
Ohmeda Medical — FDA 510(k) Submissions
Ohmeda Medical has submitted 120 FDA 510(k) premarket notifications since 1984, of which 118 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Gas-machine, Anesthesia, Incubator, Neonatal, Ventilator, Continuous, Facility Use, Warmer, Infant Radiant, Analyzer, Gas, Carbon-dioxide, Gaseous-phase . Use the specialty filter in the sidebar to narrow results.
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