FDA 510(k) Applications Submitted by GE MED. SYSTEMS ULTRASOUND & PRIM. CARE DIAG.,LLC

FDA 510(k) Number Submission Date Device Name Applicant
K040251 02/03/2004 GE LOGIQ 9 DIAGNOSTIC ULTRASOUND SYSTEM, MODEL 2404587 GE MED. SYSTEMS ULTRASOUND & PRIM. CARE DIAG.,LLC
K032656 08/28/2003 GE LOGIQ 9 ULTRASOUND BT03/IQ, MODEL 2375600-X GE MED. SYSTEMS ULTRASOUND & PRIM. CARE DIAG.,LLC


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