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FDA 510(k)

Tablo Hemodialysis System

K-Number: K200741 · 2020-03-31

Decision Date2020-03-31
Product CodeKDI
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Tablo Hemodialysis System is the device name listed in this FDA 510(k) record. The listed applicant is Outset Medical, Inc.. It received FDA 510(k) clearance on 2020-03-31 under 510(k) number K200741. The device is classified under product code KDI. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Tablo Hemodialysis System?

Tablo Hemodialysis System is a medical device that received FDA 510(k) clearance on 2020-03-31. The listed applicant is Outset Medical, Inc.. The 510(k) number is K200741.

When did Tablo Hemodialysis System receive FDA 510(k) clearance?

Tablo Hemodialysis System received FDA 510(k) clearance on 2020-03-31, under 510(k) number K200741.

Who is the listed applicant for Tablo Hemodialysis System?

The FDA 510(k) record lists Outset Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Tablo Hemodialysis System?

The FDA product code for Tablo Hemodialysis System is KDI.

Other records listing Outset Medical, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 9 devices →

Related Devices (Code: KDI)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.