DWM
- Product code
- DWM
- Device name
- Apparatus, Suction, Patient Care
- Device class
- Class 2
- 21 CFR
- 21 CFR 870.5050
- Medical specialty
- Cardiovascular
- Marketing pathway
- 510(K)
- Flag
- Third-party review eligible
- 510(k) clearances (last 3 years)
- 19
Official FDA classification page: DWM
Classification and pathway per current FDA publications. Data from openFDA (CC0).