
Interlab S.R.L.
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INTERLAB ACID HEMOGLOBIN ELECTROPHORESIS TEST SYSTEM is an FDA 510(k)-cleared medical device (K040146) manufactured by Interlab S.R.L.. This device is classified under the Hematology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 3, 2004. Regulation: 8.