meddevicedb.com FDA Device Reference

SIS BLU (SISBLU-30-01);SIS BLU (SISBLU-15-01)

K260997 Class II Traditional
Decision Date
2026-09-09
Sponsor / Applicant
Endoclot Plus Co., Ltd.

Technical Specification

510(k) Submission ID K260997
Product Code PLL
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 2026-09-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SIS BLU (SISBLU-30-01);SIS BLU (SISBLU-15-01) received FDA 510(k) clearance under submission number K260997, sponsored by Endoclot Plus Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 2026-09-09.

Classification & Regulation

This clearance is catalogued under FDA product code PLL and 21 CFR 876.1500, within the Gastroenterology, Urology review panel as a Class II device.