ACCUSIGN MOP, BIOSIGN MOP, STAUS DS MOP

ACCUSIGN MOP, BIOSIGN MOP, STAUS DS MOP is an FDA 510(k)-cleared medical device (K981771) manufactured by Princeton BioMeditech Corp.. 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 June 11, 1998. Regulation: 8.