
Ventana, Inc.
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VENTANA ER PRIMARY ANTIBODY (CLONE 6F11) is an FDA 510(k)-cleared medical device (K984567) manufactured by Ventana, Inc.. This device is classified under the Hematology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 11, 1999. Regulation: 8.