K251114
- 510(k) number
- K251114
- Device name
- FloPatch FP120
- Applicant
- Flosonics Medical CA
- Product code
- DPW — Flowmeter, Blood, Cardiovascular
- Decision date
- 2025-06-20
- Date received
- 2025-04-11
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Flag
- Third-party review
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K251114.pdf
Official FDA record: K251114
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.