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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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