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FDA 510(k)

AUTOLOGOUS BLOOD COLLECTION SET

K-Number: K923016 · 1992-11-23

ApplicantAdvanced Haemotechnologies
Decision Date1992-11-23
Product CodeCAC
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

AUTOLOGOUS BLOOD COLLECTION SET is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Haemotechnologies. It received FDA 510(k) clearance on 1992-11-23 under 510(k) number K923016. 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 AUTOLOGOUS BLOOD COLLECTION SET?

AUTOLOGOUS BLOOD COLLECTION SET is a medical device that received FDA 510(k) clearance on 1992-11-23. The listed applicant is Advanced Haemotechnologies. The 510(k) number is K923016.

When did AUTOLOGOUS BLOOD COLLECTION SET receive FDA 510(k) clearance?

AUTOLOGOUS BLOOD COLLECTION SET received FDA 510(k) clearance on 1992-11-23, under 510(k) number K923016.

Who is the listed applicant for AUTOLOGOUS BLOOD COLLECTION SET?

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

What is the FDA product code for AUTOLOGOUS BLOOD COLLECTION SET?

The FDA product code for AUTOLOGOUS BLOOD COLLECTION SET is CAC.

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Related Devices (Code: CAC)

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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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