
Phadia US, Inc.
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VARELISA RECOMBI ANA SCREEN, MODEL 12 596 is an FDA 510(k)-cleared medical device (K083188) manufactured by Phadia US, 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 March 12, 2009. Regulation: 8.