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FDA 510(k)

QBC SYSTEM HEMOGLOBIN

K-Number: K874427 · 1988-01-05

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic
Decision Date1988-01-05
Product CodeGKZ
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

QBC SYSTEM HEMOGLOBIN is the device name listed in this FDA 510(k) record. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. It received FDA 510(k) clearance on 1988-01-05 under 510(k) number K874427. The device is classified under product code GKZ. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QBC SYSTEM HEMOGLOBIN?

QBC SYSTEM HEMOGLOBIN is a medical device that received FDA 510(k) clearance on 1988-01-05. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K874427.

When did QBC SYSTEM HEMOGLOBIN receive FDA 510(k) clearance?

QBC SYSTEM HEMOGLOBIN received FDA 510(k) clearance on 1988-01-05, under 510(k) number K874427.

Who is the listed applicant for QBC SYSTEM HEMOGLOBIN?

The FDA 510(k) record lists Bd Becton Dickinson Vacutainer Systems Preanalytic as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for QBC SYSTEM HEMOGLOBIN?

The FDA product code for QBC SYSTEM HEMOGLOBIN is GKZ.

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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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