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Tablo Hemodialysis System

K211370 Class II Traditional
Decision Date
2022-07-29
Sponsor / Applicant
Outset Medical, Inc.

Technical Specification

510(k) Submission ID K211370
Product Code KDI
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5860
Decision Date 2022-07-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Tablo Hemodialysis System received FDA 510(k) clearance under submission number K211370, 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 2022-07-29.

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.