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FDA 510(k)

VIRTUAL PORTS ENDOCLEAR SYSTEM

K-Number: K080051 · 2008-03-21

ApplicantVirtual Ports, Ltd.
Decision Date2008-03-21
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

VIRTUAL PORTS ENDOCLEAR SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Virtual Ports, Ltd.. It received FDA 510(k) clearance on 2008-03-21 under 510(k) number K080051. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VIRTUAL PORTS ENDOCLEAR SYSTEM?

VIRTUAL PORTS ENDOCLEAR SYSTEM is a medical device that received FDA 510(k) clearance on 2008-03-21. The listed applicant is Virtual Ports, Ltd.. The 510(k) number is K080051.

When did VIRTUAL PORTS ENDOCLEAR SYSTEM receive FDA 510(k) clearance?

VIRTUAL PORTS ENDOCLEAR SYSTEM received FDA 510(k) clearance on 2008-03-21, under 510(k) number K080051.

Who is the listed applicant for VIRTUAL PORTS ENDOCLEAR SYSTEM?

The FDA 510(k) record lists Virtual Ports, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VIRTUAL PORTS ENDOCLEAR SYSTEM?

The FDA product code for VIRTUAL PORTS ENDOCLEAR SYSTEM is GCJ.

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.

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Other records listing Virtual Ports, Ltd. 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.

K100346ENDOCLEAR SYSTEM

Related Devices (Code: GCJ)

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.

K262397CuratOR EX2742Eizo CorporationK260884UNIDRIVE Select SystemKarl Storz SE & CO. KGK260972OEV-271MUH LCD Monitor;OEV-321MUH LCD Monitor;OEV-431MUH LCD MonitorSony CorporationK261139VereSee (VER150, VER200, VER151, VER201, VER200C, and VER-100-103)Freyja Healthcare, LLCK253541EZ-Close™ (EZ Close Port Site Closing Device, EZ Close MAX Port Site Closing Device, EZ Close II Port Site Closing Device)Medical ImpactK261614LED LCD Monitor (OEV-271H)Lg Electronics.Inc

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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