meddevicedb.com FDA Device Reference

SIS System

K230977 Class II Special
Decision Date
2023-05-02
Sponsor / Applicant
Surgical Information Sciences, Inc.

Technical Specification

510(k) Submission ID K230977
Product Code QIH
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.2050
Decision Date 2023-05-02
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SIS System received FDA 510(k) clearance under submission number K230977, sponsored by Surgical Information Sciences, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2023-05-02.

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.