MJI — Specimen/Tissue, Identification Orientation Class I
FDA product code MJI covers "Specimen/Tissue, Identification Orientation", a Class I medical device regulated under 21 CFR 864.3010. Submissions are reviewed by the Pathology panel.
Classification Details
- Product Code
- MJI
- Device Class
- Class I
- Regulation Number
- 864.3010
- Submission Type
- Review Panel
- PA
- Medical Specialty
- Pathology
- Implant
- No