
Ventrex Laboratories, Inc.
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VENTREX 125I ANTI-IGE ALLERGY ISOTOPE is an FDA 510(k)-cleared medical device (K820896) manufactured by Ventrex Laboratories, Inc.. This device is classified under the Immunology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 20, 1982. Regulation: 8.