RETICONE SYSTEM FOR EPICS XL FLOW CYTOMETRY SYSTEMS
K-Number: K990327 · 1999-04-26
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Device Summary
Frequently Asked Questions
What is the RETICONE SYSTEM FOR EPICS XL FLOW CYTOMETRY SYSTEMS?
RETICONE SYSTEM FOR EPICS XL FLOW CYTOMETRY SYSTEMS is a medical device that received FDA 510(k) clearance on 1999-04-26. The listed applicant is Coulter Corp.. The 510(k) number is K990327.
When did RETICONE SYSTEM FOR EPICS XL FLOW CYTOMETRY SYSTEMS receive FDA 510(k) clearance?
RETICONE SYSTEM FOR EPICS XL FLOW CYTOMETRY SYSTEMS received FDA 510(k) clearance on 1999-04-26, under 510(k) number K990327.
Who is the listed applicant for RETICONE SYSTEM FOR EPICS XL FLOW CYTOMETRY SYSTEMS?
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 RETICONE SYSTEM FOR EPICS XL FLOW CYTOMETRY SYSTEMS?
The FDA product code for RETICONE SYSTEM FOR EPICS XL FLOW CYTOMETRY SYSTEMS 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.
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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