The Food and Drug Administration regulates all BIA devices as class II medical devices. Manufacturers must receive clearance from the FDA to market a class II device. Please visit the FDA website for more information on RJL registration and clearances. ( FDA Website – search for RJL Systems under Applicant Name or Owner Name.)
Posted in: Analyzers, Quantum Desktop, Quantum-II, Quantum-III, Quantum-IV, Quantum-V, Quantum-X
