LMA
- Product code
- LMA
- Device name
- Digitizer, Image, Radiological
- Device class
- Class 2
- 21 CFR
- 21 CFR 892.2030
- Medical specialty
- Radiology
- Marketing pathway
- 510(K) Exempt
- 510(k) clearances (all years, FDA)
- 61 (all years; only the last 3 years are listed here)
Official FDA classification page: LMA
Classification and pathway per current FDA publications. Data from openFDA (CC0).