
Teco Diagnostics
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C-REACTIVE PROTEIN (CRP):A LATEX SLIDE TEST is an FDA 510(k)-cleared medical device (K962019) manufactured by Teco Diagnostics. This device is classified under the Immunology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 24, 1996. Regulation: 8.