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FDA 510(k)

C.A.T.S. CONTINUOUS AUTOTRANSFUSION SYSTEM

K-Number: K960006 · 1996-07-31

ApplicantFresenius AG
Decision Date1996-07-31
Product CodeCAC
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

C.A.T.S. CONTINUOUS AUTOTRANSFUSION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Fresenius AG. It received FDA 510(k) clearance on 1996-07-31 under 510(k) number K960006. The device is classified under product code CAC. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the C.A.T.S. CONTINUOUS AUTOTRANSFUSION SYSTEM?

C.A.T.S. CONTINUOUS AUTOTRANSFUSION SYSTEM is a medical device that received FDA 510(k) clearance on 1996-07-31. The listed applicant is Fresenius AG. The 510(k) number is K960006.

When did C.A.T.S. CONTINUOUS AUTOTRANSFUSION SYSTEM receive FDA 510(k) clearance?

C.A.T.S. CONTINUOUS AUTOTRANSFUSION SYSTEM received FDA 510(k) clearance on 1996-07-31, under 510(k) number K960006.

Who is the listed applicant for C.A.T.S. CONTINUOUS AUTOTRANSFUSION SYSTEM?

The FDA 510(k) record lists Fresenius AG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for C.A.T.S. CONTINUOUS AUTOTRANSFUSION SYSTEM?

The FDA product code for C.A.T.S. CONTINUOUS AUTOTRANSFUSION SYSTEM is CAC.

Related Clinical Trials

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.

Other records listing Fresenius AG 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.

Related Devices (Code: CAC)

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

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

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