Agilent Technologies Deutschland GmbH
Agilent Technologies Deutschland GmbH holds FDA 510(k) medical device clearances, first cleared 2000, most recent 2001.
Top product codes for Agilent Technologies Deutschland GmbH
Recent clearances by Agilent Technologies Deutschland GmbH
- K002758 — AGILENT COMPONENT MONITORING SYSTEM, AGILENT CARDIAC OUTPUT MODULE, AGILENT INVASIVE PRESSURE MODULE, MODEL M1175A/76A
- K003038 — AGILENT COMPONENT MONITORING SYSTEM, AGILENT V24/26, AGILENT BIS MODULE, MODEL M1175A/76A/77A,REV.L,M1205A,REV.L,M1034A
- K001722 — AGILENT COMPONENT MONITORING SYSTEM; AGILENT INVASIVE BLOOD PRESSURE MODULE
- K001333 — AGILENT COMPONENT MONITORING SYSTEM, AGILENT MULTI-MEASUREMENT SERVER AND COMPACT PORTABLE PATIENT MONITOR, AGILENT NONI
Data sourced from openFDA. This site is unofficial and independent of the FDA.