Medical Device Manufacturer · DE , Boeblingen,

Agilent Technologies Deutschland GmbH - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2000

4

Total

4

Cleared

0

Denied

FDA 510(k) Regulatory Record - Agilent Technologies Deutschland GmbH Neurology ✕

1 devices

1-1 of 1

Cleared Dec 15, 2000

AGILENT COMPONENT MONITORING SYSTEM, AGILENT V24/26, AGILENT BIS MODULE,...

Neurology · 77d