KFI — Strip, Virulence, Corynebacterium Diphtheriae Class I
FDA product code KFI covers "Strip, Virulence, Corynebacterium Diphtheriae", a Class I medical device regulated under 21 CFR 866.3140. Submissions are reviewed by the Microbiology panel.
Classification Details
- Product Code
- KFI
- Device Class
- Class I
- Regulation Number
- 866.3140
- Submission Type
- Review Panel
- MI
- Medical Specialty
- Microbiology
- Implant
- No