DRM
- Product code
- DRM
- Device name
- Compressor, Cardiac, External
- Device class
- Class 2
- 21 CFR
- 21 CFR 870.5200
- Medical specialty
- Cardiovascular
- Marketing pathway
- 510(K)
- 510(k) clearances (all years, FDA)
- 45 (all years; only the last 3 years are listed here)
Official FDA classification page: DRM
Classification and pathway per current FDA publications. Data from openFDA (CC0).