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FDA 510(k)

TRITEST REAGENT CD3 FITC/CD4 PE/CD45 PERCP

K-Number: K946055 · 1996-02-20

Decision Date1996-02-20
Product CodeGKZ
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

TRITEST REAGENT CD3 FITC/CD4 PE/CD45 PERCP is the device name listed in this FDA 510(k) record. The listed applicant is Becton Dickinson Immunocytometry Systems. It received FDA 510(k) clearance on 1996-02-20 under 510(k) number K946055. 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 TRITEST REAGENT CD3 FITC/CD4 PE/CD45 PERCP?

TRITEST REAGENT CD3 FITC/CD4 PE/CD45 PERCP is a medical device that received FDA 510(k) clearance on 1996-02-20. The listed applicant is Becton Dickinson Immunocytometry Systems. The 510(k) number is K946055.

When did TRITEST REAGENT CD3 FITC/CD4 PE/CD45 PERCP receive FDA 510(k) clearance?

TRITEST REAGENT CD3 FITC/CD4 PE/CD45 PERCP received FDA 510(k) clearance on 1996-02-20, under 510(k) number K946055.

Who is the listed applicant for TRITEST REAGENT CD3 FITC/CD4 PE/CD45 PERCP?

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

What is the FDA product code for TRITEST REAGENT CD3 FITC/CD4 PE/CD45 PERCP?

The FDA product code for TRITEST REAGENT CD3 FITC/CD4 PE/CD45 PERCP is GKZ.

Related Clinical Trials

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.

Other records listing Becton Dickinson Immunocytometry Systems as applicant

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.

View all 21 devices →

Related Devices (Code: GKZ)

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.

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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