GE Medical Systems
FDA 510(k) medical device clearances.
Clearances by GE Medical Systems — page 2
101–169 of 169- K960204 — G.E. STERILE, PERCUTANEOUS CHOLANGIOGRAPHIC TRAY
- K954874 — SPECTEF PROTOCOL
- K960141 — G.E. STERILE, STANDARD BIOPSY TRAY
- K960201 — G.E. STERILE BREAST BIOPSY/LOCALIZATION TRAY
- K960202 — G.E. STERILE PUNCTURE TRAY
- K953250 — SENOGRAPHE PEARL AND SENOGRAPHE SAPPHIRE
- K955185 — GE ADVANTAGE DICOM CR REPROCESSING STATION
- K942604 — SIGNA ADVANTAGE SP MAGNETIC RESONANCE SYSTEM
- K954666 — MPH50, MPH65, AND MPH80
- K951723 — GE B510 TRANSDUCER
- K953595 — MAGNETIC RESONANCE DIAGNOSTIC ACCESSORY
- K953832 — SOLARIX FV
- K945730 — SIGNA PROFILE
- K951144 — PHOENIX PLUS & BASE NUCLEAR MEDICINE SINGLE DETECTOR SYSTEMS
- K944979 — MAGNETIC RESONANCE DIAGNOSTIC ACCESSORY
- K941191 — REAL TIME STEREOTIX
- K950973 — MAGNETIC RESONANCE DIAGNOSTIC SYSTEM
- K930265 — HYDROGEN SPECTROSCOPY OPTION-PROBE #M1040HS/HT
- K945652 — ATTENUATION CORRECTION
- K950317 — ADVANTX 1824 SPOTFILM DEVICE
- K944013 — CT PROSPEED FAMILY
- K945375 — ADVANTX LCA
- K945842 — MOBILIX MOBILE X-RAY TABLE
- K944112 — MAGNETIC RESONANCE DIAGNOSTIC ACCESSORY
- K944967 — TOMO-LINK
- K943355 — GEMNET
- K936001 — PATLAK & FDG AUTORADIOGRAPHIC
- K940606 — HISPEED ADVANTAGE II
- K943652 — VASCULAR MP X-RAY GENERATOR
- K942120 — ADVANTAGE WINDOWS DIAGNOSTIC X-RAY WORKSTATION
- K933202 — VENUS DIAGNOSTIC ULTRASOUND SYSTEM
- K941946 — LCA ANGIOGRAPHIC IMAGING SYSTEM
- K940300 — MAGELLAN
- K936180 — TC+ SYSTEM (TILTING C-ARM SYSTEM)
- K930768 — ORION DIAGNOSTIC ULTRASOUND SYSTEM
- K934499 — MAGNETIC RESONANCE DIAGNOSTIC ACCESSORY
- K934367 — PC-MINI
- K933447 — STENOSCOP MOBILE FLUOROSCOPIC XRAY SYSTEM
- K932957 — QUANTEM (TM)
- K931049 — ADVANTX SYSTEM
- K926258 — DLX
- K923077 — ADVANTAGE WINDOWS 3D OPTION AND DENTASCAN OPTION
- K924310 — PRESTILIX 1694 D IMAGE INTENSIFIED FLUOROSCCOPIC
- K924498 — MAXXUS
- K923025 — SIGNA BREAST COIL AND ARRAY ACCESSORY
- K915138 — GE SONOCHROME
- K921192 — CT SYTEC 6000 COMPUTED TOMOGRAPHY SYSTEM
- K923309 — ARGUS PET SYSTEM
- K921777 — CARDIAC FIRST PASS ANALYSIS
- K914267 — GE 4096 PLUS & GE 2048
- K913475 — MAGNETIC RESONANCE DIAGNOSTIC DEVICE
- K912539 — SIGNA ADVANTAGE 0.5T MAGNETIC RESONANCE SYSTEM
- K911959 — SIGNA ADVANTAGE MAGNETIC RESONANCE SYSTEM M1090GF
- K910902 — VMX MOBILE X-RAY SYSTEM
- K912881 — GE MR MAX
- K910967 — NEUROCAM
- K905653 — ADVANTX AFM ANGIO SYSTEM S1808
- K911387 — CT SYTEC 4000
- K904971 — CT HILIGHT ADVANTAGE II
- K902428 — INTEGRATED DIAGNOSTIC SYSTEM W/ADD'L OPTIONS
- K903608 — V-LINK
- K903319 — MAGNETIC RESONANCE DIAGNOSTIC DEVICE
- K901730 — GE SIGNA ADVANTAGE
- K896353 — GE TARGET SERIES 2
- K895794 — GE MR MAX SYSTEM
- K894142 — ULTRANET-S COLLIMATOR
- K894269 — CT HILIGHT ADVANTAGE
- K893509 — GE SIGNA ADVANTAGE
- K892943 — MULTI PULSE POWER UNIT GENERATOR
Data sourced from openFDA. This site is unofficial and independent of the FDA.