Medical Device Manufacturer · DE , Boeblingen

Agilent Technologies, GmbH

2 submissions · 2 cleared · Since 2000
2
Total
2
Cleared
0
Denied

Agilent Technologies, GmbH — FDA 510(k) Submissions

Agilent Technologies, GmbH has submitted 2 FDA 510(k) premarket notifications since 2000, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Detector And Alarm, Arrhythmia, Analyzer, Gas, Enflurane, Gaseous-phase (anesthetic Concentration) . Use the specialty filter in the sidebar to narrow results.

2 devices
1–2 of 2
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All2 Cardiovascular 1 Anesthesiology 1