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FDA 510(k)

FLOW-COUNT COULTER FLUOROSPHERES

K-Number: K954688 · 1996-02-29

ApplicantCoulter Corp.
Decision Date1996-02-29
Product CodeGKZ
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

FLOW-COUNT COULTER FLUOROSPHERES is the device name listed in this FDA 510(k) record. The listed applicant is Coulter Corp.. It received FDA 510(k) clearance on 1996-02-29 under 510(k) number K954688. 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 FLOW-COUNT COULTER FLUOROSPHERES?

FLOW-COUNT COULTER FLUOROSPHERES is a medical device that received FDA 510(k) clearance on 1996-02-29. The listed applicant is Coulter Corp.. The 510(k) number is K954688.

When did FLOW-COUNT COULTER FLUOROSPHERES receive FDA 510(k) clearance?

FLOW-COUNT COULTER FLUOROSPHERES received FDA 510(k) clearance on 1996-02-29, under 510(k) number K954688.

Who is the listed applicant for FLOW-COUNT COULTER FLUOROSPHERES?

The FDA 510(k) record lists Coulter Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FLOW-COUNT COULTER FLUOROSPHERES?

The FDA product code for FLOW-COUNT COULTER FLUOROSPHERES 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 Coulter Corp. 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 51 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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