K254239
- 510(k) number
- K254239
- Device name
- CyClean Cord
- Applicant
- SS GLOBAL KR
- Product code
- MVL — Cord, Retraction
- Decision date
- 2026-03-27
- Date received
- 2025-12-29
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Unknown
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K254239.pdf
Official FDA record: K254239
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.