Ge Med. Systems Ultrasound & Prim. Care Diag.,Llc - FDA 510(k) Cleare...
Recent clearances: GE LOGIQ 9 DIAGNOSTIC ULTRASOUND SYSTEM, MODEL 2404587, GE LOGIQ 9 ULTRASOUND BT03/IQ, MODEL 2375600-X
2
Total
2
Cleared
0
Denied
FDA 510(k) Regulatory Record - Ge Med. Systems Ultrasound & Prim. Care Diag.,Llc Radiology ✕
2 devices