
Diagnostic Reagents, Inc.
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URINE CALIBRATORS AND CONTROLS MODIFICATION is an FDA 510(k)-cleared medical device (K935101) manufactured by Diagnostic Reagents, Inc.. This device is classified under the Clinical Toxicology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 26, 1994. Regulation: 8.