DPW
- Product code
- DPW
- Device name
- Flowmeter, Blood, Cardiovascular
- Device class
- Class 2
- 21 CFR
- 21 CFR 870.2100
- Medical specialty
- Cardiovascular
- Marketing pathway
- 510(K)
- Flag
- Third-party review eligible
- 510(k) clearances (last 3 years)
- 6
- Summaries archived here
- 6 (direct download)
- 510(k) clearances (all years, FDA)
- 138 (all years; only the last 3 years are listed here)
510(k) clearances, last 3 years (6)
| Number | Decision date | Applicant | Device name | Summary |
|---|---|---|---|---|
| K260700 | 2026-07-08 | BlueDop Medical, Ltd. | BlueDop Vascular Expert | |
| K252810 | 2026-04-24 | Flosonics Medical | FloPatch FP120 | |
| K251904 | 2025-11-20 | Remington Medical, Inc. | VascuChek Kit, VascuChek Transceiver, VascuChek Clin | |
| K251114 | 2025-06-20 | Flosonics Medical | FloPatch FP120 | |
| K243852 | 2025-04-14 | Elfi-Tech , Ltd. | Elfor-L | |
| K241583 | 2024-08-30 | Remington Medical, Inc. | VascuChek Kit, VascuChek Transceiver, VascuChek Clin |
Official FDA classification page: DPW
Classification and pathway per current FDA publications. Data from openFDA (CC0).