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FDA 510(k)

CBC/CONSTAVAC BLOOD CONSERVATION SYSTEM

K-Number: K881350 · 1988-09-30

ApplicantStryker Corp.
Decision Date1988-09-30
Product CodeCAC
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CBC/CONSTAVAC BLOOD CONSERVATION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Corp.. It received FDA 510(k) clearance on 1988-09-30 under 510(k) number K881350. 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 CBC/CONSTAVAC BLOOD CONSERVATION SYSTEM?

CBC/CONSTAVAC BLOOD CONSERVATION SYSTEM is a medical device that received FDA 510(k) clearance on 1988-09-30. The listed applicant is Stryker Corp.. The 510(k) number is K881350.

When did CBC/CONSTAVAC BLOOD CONSERVATION SYSTEM receive FDA 510(k) clearance?

CBC/CONSTAVAC BLOOD CONSERVATION SYSTEM received FDA 510(k) clearance on 1988-09-30, under 510(k) number K881350.

Who is the listed applicant for CBC/CONSTAVAC BLOOD CONSERVATION SYSTEM?

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

What is the FDA product code for CBC/CONSTAVAC BLOOD CONSERVATION SYSTEM?

The FDA product code for CBC/CONSTAVAC BLOOD CONSERVATION SYSTEM is CAC.

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Other records listing Stryker Corp. as applicant

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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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