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FDA 510(k)

GTK Trocars

K-Number: K193272 · 2020-07-09

ApplicantGuangzhou T.K Medical Instrument Co., Ltd.
Decision Date2020-07-09
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

GTK Trocars is a medical device manufactured by Guangzhou T.K Medical Instrument Co., Ltd.. It received FDA 510(k) clearance on 2020-07-09 under approval number K193272. 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 GTK Trocars?

GTK Trocars is a medical device that received FDA 510(k) clearance on 2020-07-09. It is manufactured by Guangzhou T.K Medical Instrument Co., Ltd.. The 510(k) number is K193272.

When was GTK Trocars approved by the FDA?

GTK Trocars received FDA 510(k) clearance on 2020-07-09, under approval number K193272.

What company makes GTK Trocars?

GTK Trocars is manufactured by Guangzhou T.K Medical Instrument Co., Ltd..

What is the FDA product code for GTK Trocars?

The FDA product code for GTK Trocars is GCJ.

Other Devices by Guangzhou T.K Medical Instrument Co., Ltd.

K193339GTK Veress Needles

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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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