MJL — Eia, Blastomyces Dermatitidis Class II

FDA Device Classification

FDA product code MJL covers "Eia, Blastomyces Dermatitidis", a Class II medical device regulated under 21 CFR 866.3060. Submissions are reviewed by the Microbiology panel. At least 2 recent 510(k) clearances have been granted under this product code.