
Medi-Globe Corp.
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GIP/MEDI-GLOBE SCLEROTHERAPY NEEDLES is an FDA 510(k)-cleared medical device (K955558) 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 February 28, 1996. Regulation: 8.