
Diagnostic Systems Laboratories, Inc.
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MODIFIED DSL-2300 ACTH RIA is an FDA 510(k)-cleared medical device (K900147) manufactured by Diagnostic Systems Laboratories, Inc.. This device is classified under the Clinical Chemistry specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 28, 1990. Regulation: 8.