FDA 510(k)

CLAY ADAMS QBC CENTRIFUGAL HEMOTOLOGY

K-Number: K813033 · 1982-04-09

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic

Decision Date1982-04-09

Product CodeGKG

Advisory CommitteeHE

DecisionSubstantially Equivalent

Device Summary

CLAY ADAMS QBC CENTRIFUGAL HEMOTOLOGY 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 1982-04-09 under 510(k) number K813033. The device is classified under product code GKG. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLAY ADAMS QBC CENTRIFUGAL HEMOTOLOGY?

CLAY ADAMS QBC CENTRIFUGAL HEMOTOLOGY is a medical device that received FDA 510(k) clearance on 1982-04-09. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K813033.

When did CLAY ADAMS QBC CENTRIFUGAL HEMOTOLOGY receive FDA 510(k) clearance?

CLAY ADAMS QBC CENTRIFUGAL HEMOTOLOGY received FDA 510(k) clearance on 1982-04-09, under 510(k) number K813033.

Who is the listed applicant for CLAY ADAMS QBC CENTRIFUGAL HEMOTOLOGY?

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 CLAY ADAMS QBC CENTRIFUGAL HEMOTOLOGY?

The FDA product code for CLAY ADAMS QBC CENTRIFUGAL HEMOTOLOGY is GKG.

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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.