Agilent Technologies, GmbH is one of 344 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Agilent Technologies, GmbH - FDA 510(k) Cleared Devices
Recent clearances: MODIFICATION TO AGILENT TECHNOLOGIES ANESTHESIA GAS MONITOR, MODEL M1026A #CO5
2
Total
2
Cleared
0
Denied
Agilent Technologies, GmbH has 2 FDA 510(k) cleared medical devices. Based in Boeblingen, DE.
Historical record: 2 cleared submissions from 2000 to 2000. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Agilent Technologies, GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Agilent Technologies, GmbH
2 devices