FDA product code LFG
Radioimmunoassay, Tricyclic Antidepressant Drugs
Clinical Toxicology·Class 2·21 CFR 862.3910
US regulatory classifications
- US Product Code (FDA)
- LFGView Product Code Classification →
- US Risk Class (FDA)
- Class 2
- US Regulation (CFR)
- 21 CFR 862.3910View CFR Regulation →
- Medical specialty
- Clinical Toxicology
Device characteristics
- GMP exempt
- No
- Implantable
- No
- Life-sustaining
- No
- Third party review
- Eligible
Definition
Intended to measure any of the tricyclic antidepressant drugs in serum or urine.
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About this record
Radioimmunoassay, Tricyclic Antidepressant Drugs is a medical device type in the Clinical Toxicology specialty. This page includes real-world medical device registration data worldwide for this device type, with registrations from US FDA, Brazil ANVISA, and other global markets.
View regulatory classifications, recent 510(k) clearances, active device registrations, and similar products registered globally under this device category. Pure Global AI's free directory provides comprehensive worldwide registration intelligence across 7,000+ medical device types and 21 specialties.