K251277
- 510(k) number
- K251277
- Device name
- CoraForce Microcatheter, CoraFlex Microcatheter
- Applicant
- Reflow Medical, Inc. CA · US
- Product code
- DQY — Catheter, Percutaneous
- Decision date
- 2025-08-22
- Date received
- 2025-04-24
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 3.1 MB · U.S. public domain
Also available from FDA: K251277.pdf
Official FDA record: K251277
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.