LDE
- Product code
- LDE
- Device name
- Stethoscope, Manual
- Device class
- Class 1
- 21 CFR
- 21 CFR 870.1875
- Medical specialty
- Cardiovascular
- Marketing pathway
- 510(K) Exempt
- 510(k) clearances (all years, FDA)
- 28 (all years; only the last 3 years are listed here)
Official FDA classification page: LDE
Classification and pathway per current FDA publications. Data from openFDA (CC0).