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FDA 510(k)

easyPPHTM Hemorrhoidal Stapler for Single Use

K-Number: K183477 · 2019-02-11

Decision Date2019-02-11
Product CodeGDW
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

easyPPHTM Hemorrhoidal Stapler for Single Use is a medical device manufactured by Ezisurg Medical Co., Ltd.. It received FDA 510(k) clearance on 2019-02-11 under approval number K183477. The device is classified under product code GDW. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the easyPPHTM Hemorrhoidal Stapler for Single Use?

easyPPHTM Hemorrhoidal Stapler for Single Use is a medical device that received FDA 510(k) clearance on 2019-02-11. It is manufactured by Ezisurg Medical Co., Ltd.. The 510(k) number is K183477.

When was easyPPHTM Hemorrhoidal Stapler for Single Use approved by the FDA?

easyPPHTM Hemorrhoidal Stapler for Single Use received FDA 510(k) clearance on 2019-02-11, under approval number K183477.

What company makes easyPPHTM Hemorrhoidal Stapler for Single Use?

easyPPHTM Hemorrhoidal Stapler for Single Use is manufactured by Ezisurg Medical Co., Ltd..

What is the FDA product code for easyPPHTM Hemorrhoidal Stapler for Single Use?

The FDA product code for easyPPHTM Hemorrhoidal Stapler for Single Use is GDW.

Related Clinical Trials

Other Devices by Ezisurg Medical Co., Ltd.

Related Devices (Code: GDW)

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.