LPI — Kit, Assay, Progesterone Receptor Class III
FDA product code LPI covers "Kit, Assay, Progesterone Receptor", a Class III medical device regulated under 21 CFR 864.1860. Submissions are reviewed by the Hematology panel.
Classification Details
- Product Code
- LPI
- Device Class
- Class III
- Regulation Number
- 864.1860
- Submission Type
- Review Panel
- CH
- Medical Specialty
- Hematology
- Implant
- No