K232536
- 510(k) number
- K232536
- Device name
- Soldier Microcatheter
- Applicant
- Embolx, Inc. CA · US
- Product code
- DQO — Catheter, Intravascular, Diagnostic
- Decision date
- 2024-02-23
- Date received
- 2023-08-21
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K232536.pdf
Official FDA record: K232536
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.