GOZ — Antisera, Fluorescent, B. Pertussis Class I

FDA Device Classification

FDA product code GOZ covers "Antisera, Fluorescent, B. Pertussis", a Class I medical device regulated under 21 CFR 866.3065. Submissions are reviewed by the Microbiology panel.

Classification Details

Product Code
GOZ
Device Class
Class I
Regulation Number
866.3065
Submission Type
Review Panel
MI
Medical Specialty
Microbiology
Implant
No