DLB
- Product code
- DLB
- Device name
- Radioimmunoassay, Lsd (125-I)
- Device class
- Class 2
- 21 CFR
- 21 CFR 862.3580
- Medical specialty
- Clinical Toxicology
- Marketing pathway
- 510(K)
- Flag
- Third-party review eligible
- 510(k) clearances (last 3 years)
- 7
Official FDA classification page: DLB
Classification and pathway per current FDA publications. Data from openFDA (CC0).