meddevicedb.com FDA Device Reference

CyClean Cord

K254239 Traditional
Decision Date
2026-03-27
Sponsor / Applicant
SS GLOBAL

Technical Specification

510(k) Submission ID K254239
Product Code MVL
Medical Specialty / Panel Unknown
Decision Date 2026-03-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CyClean Cord received FDA 510(k) clearance under submission number K254239, sponsored by SS GLOBAL. The device was reviewed via the Traditional premarket notification pathway and assigned to the Unknown review panel. The statutory decision date of record is 2026-03-27.

Classification & Regulation

This clearance is catalogued under FDA product code MVL , within the Unknown review panel as a device.