MJD — Culture Media, Antimycobacteria, Susceptibility Test Class II

FDA Device Classification

FDA product code MJD covers "Culture Media, Antimycobacteria, Susceptibility Test", a Class II medical device regulated under 21 CFR 866.1700. Submissions are reviewed by the Microbiology panel. At least 3 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
MJD
Device Class
Class II
Regulation Number
866.1700
Submission Type
Review Panel
MI
Medical Specialty
Microbiology
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K920143remelTB SUSCEPTIBILITY QUADS I AND IIJune 9, 1992
K840981remelNIACIN REAGENT STRIPMarch 23, 1984
K823859gibco laboratories life technologiesMIDDLEBROOK 7H10 AGAR BASE-LOWPHMarch 8, 1983