
Dynatech Laboratories, Inc.
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DYNATECH SPD 3000, #002-900-0000 is an FDA 510(k)-cleared medical device (K872363) manufactured by Dynatech Laboratories, Inc.. This device is classified under the Clinical Chemistry specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on July 15, 1987. Regulation: 8.