MCG — Dna-Probe, Agent, Listeria Class I

FDA Device Classification

FDA product code MCG covers "Dna-Probe, Agent, Listeria", a Class I medical device regulated under 21 CFR 866.3355. Submissions are reviewed by the Microbiology panel.

Classification Details

Product Code
MCG
Device Class
Class I
Regulation Number
866.3355
Submission Type
Review Panel
MI
Medical Specialty
Microbiology
Implant
No