Medi-Globe Corp.
MODIFICATION OF GIP/MEDI-GLOBE ULTRASOUND NEEDLE SYSTEM
SKU K990220UPC FCG
In Stock
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IIFDA 510(k) Cleared (K990220)
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Free shipping on orders over $99 · 30-day returns
Medi-Globe Corp.
Free shipping on orders over $99 · 30-day returns
MODIFICATION OF GIP/MEDI-GLOBE ULTRASOUND NEEDLE SYSTEM is an FDA 510(k)-cleared medical device (K990220) manufactured by Medi-Globe Corp.. 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 30, 1999. Regulation: 8.
