ALASTAT MICROPLATE LATEX-SPECIFIC IGE ALLERGEN

ALASTAT MICROPLATE LATEX-SPECIFIC IGE ALLERGEN is an FDA 510(k)-cleared medical device (K953014) manufactured by Diagnostic Products Corp.. This device is classified under the Immunology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 14, 1995. Regulation: 8.