K242692
- 510(k) number
- K242692
- Device name
- SteadiSet Infusion Set
- Applicant
- Capillary Biomedical, LLC CA · US
- Product code
- FPA — Set, Administration, Intravascular
- Decision date
- 2025-05-09
- Date received
- 2024-09-09
- Decision
- Substantially Equivalent
- Clearance type
- Abbreviated
- Advisory committee
- General Hospital
PDFDownload 510(k) SummaryArchived here · 0.3 MB · U.S. public domain
Also available from FDA: K242692.pdf
Official FDA record: K242692
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.