Ge Medical Systems, Inc.
Ge Medical Systems, Inc. holds FDA 510(k) medical device clearances, first cleared 1997, most recent 2009.
Top product codes for Ge Medical Systems, Inc.
Recent clearances by Ge Medical Systems, Inc.
- K091673 — GE LIGHTSPEED ACT FP16
- K082104 — GE LIGHTSPEED RT16 / LIGHTSPEED XTRA V2 CT SYSTEM (AKA GE LIGHTSPEED RT16 / LIGHTSPEED XTRA CT SYSTEM
- K042844 — GE SIGNA EXCITE 1.5T 6 CHANNEL PHASED ARRAY FLEX COIL, GE SIGNA EXCITE 3.0T 6 CHANNEL PHASED ARRAY FLEX COIL
- K042053 — INNOVA 4100, INNOVA 3100
- K040125 — SENOGRAPHIC STEREO
- K033244 — DIGITAL FLUOROSCOPIC IMAGING SYSTEM, MODEL INNOVA 4100 WITH TILT TABLE OPTION
- K031209 — GE 1.5T 8 CHANNEL TORSO COIL
- K023943 — CT COLONOGRAPHY
- K030934 — GE LOGIQ 9 MODEL 2375600
- K030953 — GE 3.0T GENERAL PURPOSE FLEX COIL
- K030495 — 3.0T TORSO PHASED ARRAY COIL
- K024200 — INNOVA 2000 AND INNOVA 2000S (MOBILE VERSION)
- K024137 — JUPITER PROCESSING AND REVIEW WORKSTATION
- K023178 — INNOVA 4100
- K022322 — INNOVA AND INNOVA 2000 S
- K022240 — MOBILE MILLENNIUM MG SYSTEM
- K022310 — ADVANTAGE WINDOWS X-RAY/MR FUSION
- K021491 — HISPEED DUAL
- K011604 — PROSTATE SPECTROSCOPY AND IMAGING EXAM (PROSE) SOFTWARE OPTION FOR MRI
- K012385 — HISPEED X/I SMART GANTRY OPTION
- K012389 — REVOLUTION XR/D DIGITAL RADIOGRAPHIC IMAGING SYSTEM
- K012313 — CT COLONOGRAPHY/NAVIGATOR2
- K010641 — GE CT-PET SYSTEM
- K010336 — ADVANTAGE WINDOWS CT/PET FUSION
- K003573 — DIFFUSION TENSOR IMAGING OPTION
- K003931 — VIVID 7 WITH SONOPAC, MODEL FB0008XX
- K003849 — GE ADVANCE NXI PET SYSTEM
- K001946 — NEUROVASCULAR ARRAY COIL
- K001267 — GE SYSTEM FIVE
- K000516 — GE LOGIQ 700
- K000695 — GE DOLPHIN DIAGNOSTIC ULTRASOUND SYSTEM, ULTRASONIC PULSED DOPPLER IMAGING SYSTEM
- K000300 — LIGHTSPEED 2.0CT SCANNER SYSTEM
- K993037 — LCV+ VERSION 2
- K993645 — CT/E COMPUTED TOMOGRAPHY SCANNNER SYSTEM
- K993791 — CT PERFUSION OPTION
- K993792 — SMART VESSEL ANALYSIS (SMART VA) OPTION
- K993665 — LEGEND CRF FLUORO AND RAD SYSTEM
- K992746 — SIGNA HFO/I MAGNETIC RESONANCE SYSTEM
- K993364 — GE LOGIQ 700 WITH CODED EXCITATION MODIFICATION
- K993365 — GE LOGIQ 700 WITH HARMONIC IMAGING MODIFICATION
- K993090 — SILHOUETTE FC
- K992135 — SIGNA PROFILE/I MAGNETIC RESONANCE SYSTEM
- K991629 — GE VIEW APPLICATIONS (CONSISTING OF GE VIEWING STATION AND GE EXTENDED VIEWING STATION) VERSION 1.2C
- K992208 — GE LOGIQ 200 MD DIAGNOSTIC ULTRASOUND SYSTEM
- K991716 — HISPEED NX/I CT SCANNER SYSTEM
- K990550 — 3.0T SIGNA VH/I MAGNETIC RESONANCE SYSTEM
- K990226 — GE LOGIQ700 DIAGNOSTIC ULTRASOUND SYSTEM WITH B-FLOW
- K982772 — SIGNA PROFILE QUADRATURE THORACIC/LUMBAR SPINE PHASED ARRAY COIL
- K973270 — LEG'MAP OPTION
- K973368 — STRAIT'MAP OPTION
- K972704 — KINEMATIC POSITIONERS
- K972399 — ADVANTAGE WINDOWS VOLUME RENDERING OPTION
- K972296 — MAGNETIC RESONANCE DIAGNOSTIC SYSTEM
- K970628 — GE ADVANTAGE DIGITIZER WORKSTATION
Data sourced from openFDA. This site is unofficial and independent of the FDA.