
Ge Med. Systems Ultrasound & Prim. Care Diag.,Llc
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GE LOGIQ 9 DIAGNOSTIC ULTRASOUND SYSTEM, MODEL 2404587 is an FDA 510(k)-cleared medical device (K040251) manufactured by Ge Med. Systems Ultrasound & Prim. Care Diag.,Llc. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 19, 2004. Regulation: 8.