GTF — Antisera, Bethesda - Ballerup Polyvalent, Citrobacter Spp. Class I

FDA Device Classification

FDA product code GTF covers "Antisera, Bethesda - Ballerup Polyvalent, Citrobacter Spp.", a Class I medical device regulated under 21 CFR 866.3125. Submissions are reviewed by the Microbiology panel.

Classification Details

Product Code
GTF
Device Class
Class I
Regulation Number
866.3125
Submission Type
Review Panel
MI
Medical Specialty
Microbiology
Implant
No