meddevicedb.com FDA Device Reference

Sequential Compression System (SCD600)

K250190 Class II Traditional
Decision Date
2025-12-08
Sponsor / Applicant
Shenzhen Comen Medical Instruments Co.,Ltd

Technical Specification

510(k) Submission ID K250190
Product Code JOW
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.5800
Decision Date 2025-12-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Sequential Compression System (SCD600) received FDA 510(k) clearance under submission number K250190, sponsored by Shenzhen Comen Medical Instruments Co.,Ltd. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2025-12-08.

Classification & Regulation

This clearance is catalogued under FDA product code JOW and 21 CFR 870.5800, within the Cardiovascular review panel as a Class II device.