
Bivona Medical Technologies
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MODIFIED PORGES SPEC 5* SUPRAPUBIC CATHETER is an FDA 510(k)-cleared medical device (K901603) manufactured by Bivona Medical Technologies. 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 May 3, 1990. Regulation: 8.