MDJ — Reagents, Cysticercosis Class I

FDA Device Classification

FDA product code MDJ covers "Reagents, Cysticercosis", a Class I medical device regulated under 21 CFR 866.3200. Submissions are reviewed by the Microbiology panel. At least 1 recent 510(k) clearance has been granted under this product code.

Classification Details

Product Code
MDJ
Device Class
Class I
Regulation Number
866.3200
Submission Type
Review Panel
MI
Medical Specialty
Microbiology
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K900780lmd laboratoriesCYSTICERCOSIS SEROLOGICAL REAGENTSOctober 4, 1990