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FDA 510(k)

QBC CENTRIFUGAL HEMATOLOGY SYS

K-Number: K830451 · 1983-04-27

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic
Decision Date1983-04-27
Product CodeGKL
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

QBC CENTRIFUGAL HEMATOLOGY SYS 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 1983-04-27 under 510(k) number K830451. The device is classified under product code GKL. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QBC CENTRIFUGAL HEMATOLOGY SYS?

QBC CENTRIFUGAL HEMATOLOGY SYS is a medical device that received FDA 510(k) clearance on 1983-04-27. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K830451.

When did QBC CENTRIFUGAL HEMATOLOGY SYS receive FDA 510(k) clearance?

QBC CENTRIFUGAL HEMATOLOGY SYS received FDA 510(k) clearance on 1983-04-27, under 510(k) number K830451.

Who is the listed applicant for QBC CENTRIFUGAL HEMATOLOGY SYS?

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 CENTRIFUGAL HEMATOLOGY SYS?

The FDA product code for QBC CENTRIFUGAL HEMATOLOGY SYS is GKL.

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Related Devices (Code: GKL)

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.

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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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