DTW
- Product code
- DTW
- Device name
- Monitor And/Or Control, Level Sensing, Cardiopulmonary Bypass
- Device class
- Class 2
- 21 CFR
- 21 CFR 870.4340
- Medical specialty
- Cardiovascular
- Marketing pathway
- 510(K) Exempt
- 510(k) clearances (all years, FDA)
- 17 (all years; only the last 3 years are listed here)
Official FDA classification page: DTW
Classification and pathway per current FDA publications. Data from openFDA (CC0).