meddevicedb.com FDA Device Reference

SIS Software Version 3.6.0

K192304 Class II Special
Decision Date
2019-09-13
Sponsor / Applicant
Surgical Information Sciences, Inc.

Technical Specification

510(k) Submission ID K192304
Product Code LLZ
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.2050
Decision Date 2019-09-13
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SIS Software Version 3.6.0 received FDA 510(k) clearance under submission number K192304, 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 2019-09-13.

Classification & Regulation

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