STC DIAGNOSTIC AUTO-LYTE PROPOXYPHENE EIA

STC DIAGNOSTIC AUTO-LYTE PROPOXYPHENE EIA is an FDA 510(k)-cleared medical device (K944372) manufactured by Solarcare, 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 February 7, 1995. Regulation: 8.