CATSmart, Automated Blood Processing Autotransfusion System

FDA 510(k) K210089 · Fresenius Kabi AG

Substantially Equivalent

510(k) numberK210089

Submission

Device name
CATSmart, Automated Blood Processing Autotransfusion System
Applicant
Fresenius Kabi AG
Bad Homburg, DE
Received
January 13, 2021
Decision date
February 11, 2021
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
CAC – Apparatus, Autotransfusion
Device class
Class II (moderate risk)
Regulation
21 CFR 868.5830
Specialty
Anesthesiology
Life-sustaining
Yes

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Questions and answers

When was CATSmart, Automated Blood Processing Autotransfusion System cleared by the FDA?

CATSmart, Automated Blood Processing Autotransfusion System (K210089) received a 510(k) decision of Substantially Equivalent on February 11, 2021, 29 days after the submission was received.

What is the product code of K210089?

The FDA product code is CAC – Apparatus, Autotransfusion, a Class II (moderate risk) device regulated under 21 CFR 868.5830.