TRITEST REAGENT CD3 FITC/CD4 PE/CD45 PERCP
K-Number: K946055 · 1996-02-20
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Device Summary
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.
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
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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