
Streck Laboratories, Inc.
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PARA 12 PLUS RETICS is an FDA 510(k)-cleared medical device (K000945) manufactured by Streck Laboratories, 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 April 17, 2000. Regulation: 8.