FDA 510(k)

HEMATOLOGY QUALITY CONTROL MIXTURE

K-Number: K823930 · 1983-02-01

Decision Date1983-02-01

Product CodeGJP

Advisory CommitteeHE

DecisionSubstantially Equivalent

Device Summary

HEMATOLOGY QUALITY CONTROL MIXTURE is the device name listed in this FDA 510(k) record. The listed applicant is Fisher Scientific Co., LLC. It received FDA 510(k) clearance on 1983-02-01 under 510(k) number K823930. The device is classified under product code GJP. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HEMATOLOGY QUALITY CONTROL MIXTURE?

HEMATOLOGY QUALITY CONTROL MIXTURE is a medical device that received FDA 510(k) clearance on 1983-02-01. The listed applicant is Fisher Scientific Co., LLC. The 510(k) number is K823930.

When did HEMATOLOGY QUALITY CONTROL MIXTURE receive FDA 510(k) clearance?

HEMATOLOGY QUALITY CONTROL MIXTURE received FDA 510(k) clearance on 1983-02-01, under 510(k) number K823930.

Who is the listed applicant for HEMATOLOGY QUALITY CONTROL MIXTURE?

The FDA 510(k) record lists Fisher Scientific Co., LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HEMATOLOGY QUALITY CONTROL MIXTURE?

The FDA product code for HEMATOLOGY QUALITY CONTROL MIXTURE is GJP.

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Other records listing Fisher Scientific Co., LLC 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.