
Inova Diagnostics, Inc.
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QUANTA FLASH (TM) DGP SCREEN is an FDA 510(k)-cleared medical device (K111414) manufactured by Inova Diagnostics, 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 October 19, 2011. Regulation: 8.