meddevicedb.com FDA Device Reference

Tablo Console

K160881 Class II Traditional
Decision Date
2016-11-15
Sponsor / Applicant
Outset Medical, Inc.

Technical Specification

510(k) Submission ID K160881
Product Code KDI
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5860
Decision Date 2016-11-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Tablo Console received FDA 510(k) clearance under submission number K160881, sponsored by Outset Medical, Inc.. 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 2016-11-15.

Classification & Regulation

This clearance is catalogued under FDA product code KDI and 21 CFR 876.5860, within the Gastroenterology, Urology review panel as a Class II device.