MIV — Immunofluorescent Assay, T. Cruzi Class I
FDA product code MIV covers "Immunofluorescent Assay, T. Cruzi", a Class I medical device regulated under 21 CFR 866.3870. Submissions are reviewed by the Microbiology panel.
Classification Details
- Product Code
- MIV
- Device Class
- Class I
- Regulation Number
- 866.3870
- Submission Type
- Review Panel
- MI
- Medical Specialty
- Microbiology
- Implant
- No