meddevicedb.com FDA Device Reference

SIS System

K241083 Class II Traditional
Decision Date
2024-06-14
Sponsor / Applicant
Surgical Information Sciences, Inc.

Technical Specification

510(k) Submission ID K241083
Product Code QIH
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.2050
Decision Date 2024-06-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SIS System received FDA 510(k) clearance under submission number K241083, sponsored by Surgical Information Sciences, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2024-06-14.

Classification & Regulation

This clearance is catalogued under FDA product code QIH and 21 CFR 892.2050, within the Radiology review panel as a Class II device.