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FDA 510(k)

FACSORT FLOW CYTOMETER

K-Number: K923790 · 1993-09-01

Decision Date1993-09-01
Product CodeGKZ
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

FACSORT FLOW CYTOMETER 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 1993-09-01 under 510(k) number K923790. 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 FACSORT FLOW CYTOMETER?

FACSORT FLOW CYTOMETER is a medical device that received FDA 510(k) clearance on 1993-09-01. The listed applicant is Becton Dickinson Immunocytometry Systems. The 510(k) number is K923790.

When did FACSORT FLOW CYTOMETER receive FDA 510(k) clearance?

FACSORT FLOW CYTOMETER received FDA 510(k) clearance on 1993-09-01, under 510(k) number K923790.

Who is the listed applicant for FACSORT FLOW CYTOMETER?

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 FACSORT FLOW CYTOMETER?

The FDA product code for FACSORT FLOW CYTOMETER 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

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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