Ge Medical Systems, LLC

Ge Medical Systems, LLC holds 105 FDA 510(k) medical device clearances, first cleared 2003, most recent 2026, with 168 FDA device recalls on record.

Clearances by Ge Medical Systems, LLC — page 2

101–105 of 105

K041476 — GE SIGNA EXCITE 1.5T MR SYSTEM, GE SIGNA EXCITE 3.0T MR SYSTEMCode LNH·2004-06-17
K040372 — LIGHTSPEED 7.0 CT SCANNER SYSTEMCode JAK·2004-03-01
K033502 — LIGHTSPEED 6.0 CT SCANNER SYSTEMCode JAK·2003-11-20
K032915 — ADVANTAGE 4D OPTIONCode JAK·2003-10-30
K032795 — GE 0.7T SIGNA OPENSPEED WITH EXCITE MR SYSTEMCode LNH·2003-10-08

Data sourced from openFDA. This site is unofficial and independent of the FDA.