Ge Medical Systems F.I. Haifa
Ge Medical Systems F.I. Haifa holds FDA 510(k) medical device clearances, first cleared 1998, most recent 2013.
Top product codes for Ge Medical Systems F.I. Haifa
Recent clearances by Ge Medical Systems F.I. Haifa
- K130884 — XELERIS 3.1 PROCESSING AND REVIEW WORKSTATION
- K093982 — XELERIS 3 PROCESSING AND REVIEW WORKSTATION
- K093514 — DISCOVERY MODEL NM/CT 670
- K083504 — GE DISCOVERY NM/CT 570C
- K080124 — VENTRI 1.1
- K051855 — VENTRI
- K043381 — INFINIA LIGHTSPEED
- K033874 — MYOLIGHT
- K023932 — GE PHOTON ENERGY RECOVERY (PER) OPTION
- K022960 — GE QUASAR NUCLEAR MEDICINE SYSTEM
- K003264 — QPS/BPGS/MOCO PROCESSING APPLICATIONS FOR ENTEGRA WORKSTATION
- K000395 — EINSTEIN PROCESSING AND REVIEW WORKSTATION
- K994167 — CODE AC: ATTENUATION CORRECTION SYSTEM FOR DUAL-HEAD VARIABLE-ANGLE GAMMA CAMERA WITH COINCIDENCE OPTION (CODE)
- K991841 — HAWKEYE OPTION FOR DUAL-HEAD VARIABLE ANGLE GAMMA CAMERA
- K991896 — MG ATC: ATTENUATION CORRECTION SYSTEM FOR DUAL-HEAD VARIABLE-ANGLE GAMMA CAMERA
- K981352 — VPC-94 ULTRA HIGH ENERGY COLLIMATERS MODEL NUMBERS 480-685-9402
- K980959 — VTRANSACT: ATTENUATION CORRECTION SYSTEM FOR DUAL-HEAD VARIABLE ANGLE GAMMA CAMERA
Data sourced from openFDA. This site is unofficial and independent of the FDA.