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FDA 510(k)

HEMOVAC BLOOD REINFUSION SYSTEM

K-Number: K041525 · 2004-10-14

ApplicantZimmer, Inc.
Decision Date2004-10-14
Product CodeCAC
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

HEMOVAC BLOOD REINFUSION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Zimmer, Inc.. It received FDA 510(k) clearance on 2004-10-14 under 510(k) number K041525. 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 HEMOVAC BLOOD REINFUSION SYSTEM?

HEMOVAC BLOOD REINFUSION SYSTEM is a medical device that received FDA 510(k) clearance on 2004-10-14. The listed applicant is Zimmer, Inc.. The 510(k) number is K041525.

When did HEMOVAC BLOOD REINFUSION SYSTEM receive FDA 510(k) clearance?

HEMOVAC BLOOD REINFUSION SYSTEM received FDA 510(k) clearance on 2004-10-14, under 510(k) number K041525.

Who is the listed applicant for HEMOVAC BLOOD REINFUSION SYSTEM?

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

What is the FDA product code for HEMOVAC BLOOD REINFUSION SYSTEM?

The FDA product code for HEMOVAC BLOOD REINFUSION SYSTEM is CAC.

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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.

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