
Latex Ind., Inc.
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BLADDER RETENTION CATHETERIZATION TRAY is an FDA 510(k)-cleared medical device (K791674) manufactured by Latex Ind., Inc.. 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 November 4, 1979. Regulation: 8.