Medi-Globe Corporation
SONOTIP II 25-GAUGE ULTRASOUND NEEDLE SYSTEM, MODELS GUS-01-18-025 AND GUS-01-27-025
SKU K083802UPC FCG
In Stock
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IIFDA 510(k) Cleared (K083802)
1
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Medi-Globe Corporation
Free shipping on orders over $99 · 30-day returns
SONOTIP II 25-GAUGE ULTRASOUND NEEDLE SYSTEM, MODELS GUS-01-18-025 AND GUS-01-27-025 is an FDA 510(k)-cleared medical device (K083802) manufactured by Medi-Globe Corporation. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 19, 2009. Regulation: 8.
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