K260700
- 510(k) number
- K260700
- Device name
- BlueDop Vascular Expert
- Applicant
- BlueDop Medical, Ltd. GB
- Product code
- DPW — Flowmeter, Blood, Cardiovascular
- Decision date
- 2026-07-08
- Date received
- 2026-03-04
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K260700.pdf
Official FDA record: K260700
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.