FDA 510(k) Applications Submitted by AGILENT TECHNOLOGIES DEUTSCHLAND GMBH
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K001333 |
04/27/2000 |
AGILENT COMPONENT MONITORING SYSTEM, AGILENT MULTI-MEASUREMENT SERVER AND COMPACT PORTABLE PATIENT MONITOR, AGILENT NONI |
AGILENT TECHNOLOGIES DEUTSCHLAND GMBH |
K001722 |
06/06/2000 |
AGILENT COMPONENT MONITORING SYSTEM; AGILENT INVASIVE BLOOD PRESSURE MODULE |
AGILENT TECHNOLOGIES DEUTSCHLAND GMBH |
K002758 |
09/05/2000 |
AGILENT COMPONENT MONITORING SYSTEM, AGILENT CARDIAC OUTPUT MODULE, AGILENT INVASIVE PRESSURE MODULE, MODEL M1175A/76A |
AGILENT TECHNOLOGIES DEUTSCHLAND GMBH |
K003038 |
09/29/2000 |
AGILENT COMPONENT MONITORING SYSTEM, AGILENT V24/26, AGILENT BIS MODULE, MODEL M1175A/76A/77A,REV.L,M1205A,REV.L,M1034A |
AGILENT TECHNOLOGIES DEUTSCHLAND GMBH |
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