
Serono-Baker Diagnostics, Inc.
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SRI DIGOXIN ENZYME IMMUNOASSAY is an FDA 510(k)-cleared medical device (K915602) manufactured by Serono-Baker Diagnostics, 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 16, 1992. Regulation: 8.