Agilent Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: GenetiSure Dx Postnatal Assay, MODIFICATION TO DEVICE LINK SYSTEM, MODEL M2376A, AGILENT M2636B TELEMON B MONITOR (TELEMON B)
30
Total
30
Cleared
0
Denied
FDA 510(k) Regulatory Record - Agilent Technologies, Inc. Radiology ✕
3 devices