meddevicedb.com FDA Device Reference

Tablo Cartridge

K210782 Class II Traditional
Decision Date
2021-11-26
Sponsor / Applicant
Outset Medical, Inc.

Technical Specification

510(k) Submission ID K210782
Product Code FJK
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5820
Decision Date 2021-11-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Tablo Cartridge received FDA 510(k) clearance under submission number K210782, 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 2021-11-26.

Classification & Regulation

This clearance is catalogued under FDA product code FJK and 21 CFR 876.5820, within the Gastroenterology, Urology review panel as a Class II device.