JLE — Radioimmunoassay, Desoxycorticosterone Class I
FDA product code JLE covers "Radioimmunoassay, Desoxycorticosterone", a Class I medical device regulated under 21 CFR 862.1250. Submissions are reviewed by the Clinical Chemistry panel.
Classification Details
- Product Code
- JLE
- Device Class
- Class I
- Regulation Number
- 862.1250
- Submission Type
- Review Panel
- CH
- Medical Specialty
- Clinical Chemistry
- Implant
- No