Philips Ultrasound, Inc.
CX50 VERSION 2.0 DIAGNOSTIC ULTRASOUND SYSTEM AND TRANSDUCERS
SKU K091804UPC ITX
In Stock
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IIFDA 510(k) Cleared (K091804)
1
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Philips Ultrasound, Inc.
Free shipping on orders over $99 · 30-day returns
CX50 VERSION 2.0 DIAGNOSTIC ULTRASOUND SYSTEM AND TRANSDUCERS is an FDA 510(k)-cleared medical device (K091804) manufactured by Philips Ultrasound, Inc.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 16, 2009. Regulation: 8.
