FDA 510(k)

VIKY

K-Number: K082233 · 2008-12-18

Decision Date2008-12-18

Product CodeGCJ

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

VIKY is the device name listed in this FDA 510(k) record. The listed applicant is Endocontrol. It received FDA 510(k) clearance on 2008-12-18 under 510(k) number K082233. 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 VIKY?

VIKY is a medical device that received FDA 510(k) clearance on 2008-12-18. The listed applicant is Endocontrol. The 510(k) number is K082233.

When did VIKY receive FDA 510(k) clearance?

VIKY received FDA 510(k) clearance on 2008-12-18, under 510(k) number K082233.

Who is the listed applicant for VIKY?

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

What is the FDA product code for VIKY?

The FDA product code for VIKY is GCJ.

Other records listing Endocontrol 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.

K122820VIKY UP

Related Devices (Code: GCJ)

K262397CuratOR EX2742Eizo Corporation K260884UNIDRIVE Select SystemKarl Storz SE & CO. KG K260972OEV-271MUH LCD Monitor;OEV-321MUH LCD Monitor;OEV-431MUH LCD MonitorSony Corporation K261139VereSee (VER150, VER200, VER151, VER201, VER200C, and VER-100-103)Freyja Healthcare, LLC K253541EZ-Close™ (EZ Close Port Site Closing Device, EZ Close MAX Port Site Closing Device, EZ Close II Port Site Closing Device)Medical Impact K261614LED 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.