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Agilent Technologies, Inc.

FDA 510(k) & PMA Approved Devices — 30 products

Total Devices30
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K163367 GenetiSure Dx Postnatal AssayPFX2017-08-11 View
510(k) K012094 MODIFICATION TO DEVICE LINK SYSTEM, MODEL M2376AMWI2001-07-20 View
510(k) K011824 AGILENT M2636B TELEMON B MONITOR (TELEMON B)DSI2001-07-02 View
510(k) K010634 HEARTSTREAM XL DEFIBIBRILLATOR/MONITOR, MODEL M4735A, HEARTSTREAM XLT DEFIBRILLATOR/MONITOR.MODEL M2500BMKJ2001-06-11 View
510(k) K011578 M2376A DEVICELINK SYSTEM, MODEL M2376AMWI2001-06-08 View
510(k) K003819 HEARTSTREAM ATTENUATED DEFIBRILLATION PADS, MODEL M3870AMKJ2001-05-02 View
510(k) K011093 AGILENT INFORMATION CENTER SOFTWARE FOR M3150,M3151,M3153 AND M3154MHX2001-05-01 View
510(k) K010453 M2376A DEVICELINK SYSTEMMWI2001-03-02 View
510(k) K010342 M2376A DEVICELINK SYSTEM, MODEL M2376AMWI2001-02-14 View
510(k) K010048 M2376A DEVICELINK SYSTEMMWI2001-02-01 View
510(k) K003565 HEARTSTREAM FR2 AED, MODEL M3860A,M3861AMKJ2000-12-20 View
510(k) K003621 ST/AR ST AND ARRHYTHMIA SOFTWARE, MODEL RELEASE D.0MHX2000-12-20 View
510(k) K003622 M2376A DEVICELINK SYSTEM, MODEL M2376AMWI2000-12-18 View
510(k) K002459 PAGEWRITER 10/10I, MODEL M2662A HANDHELD ELECTROCARDIOGRAPHDPS2000-11-08 View
510(k) K003107 M2376A DEVICELINK SYSTEMMWI2000-10-19 View
510(k) K002967 M2376A DEVICELINK SYSTEM, MODEL M2376AMWI2000-10-18 View
510(k) K002470 M2424A SONOS 5500/4500 DIAGNOSTIC ULTRASOUND SYSTEM, VERSION B.2. 21330A TRANSDUCERIYN2000-09-08 View
510(k) K001725 HEARTSTREAM XL DEFIBRILLATOR/MONITOR, MODEL M4735AMKJ2000-09-08 View
510(k) K002397 M2430 DIAGNOSTIC ULTRASOUND SYSTEM WITH THE 21420 TRANSDUCERIYN2000-08-17 View
510(k) K002009 HP M2376A DEVICE LINK SYSTEM, MODEL M2376AMWI2000-08-02 View
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