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FDA 510(k)

Disposable Powered Articulating Endoscopic Linear Cutter Stapler & Reloads

K-Number: K202467 · 2020-12-14

Decision Date2020-12-14
Product CodeGDW
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Disposable Powered Articulating Endoscopic Linear Cutter Stapler & Reloads is a medical device manufactured by Fengh Medical Co., Ltd.. It received FDA 510(k) clearance on 2020-12-14 under approval number K202467. 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 Disposable Powered Articulating Endoscopic Linear Cutter Stapler & Reloads?

Disposable Powered Articulating Endoscopic Linear Cutter Stapler & Reloads is a medical device that received FDA 510(k) clearance on 2020-12-14. It is manufactured by Fengh Medical Co., Ltd.. The 510(k) number is K202467.

When was Disposable Powered Articulating Endoscopic Linear Cutter Stapler & Reloads approved by the FDA?

Disposable Powered Articulating Endoscopic Linear Cutter Stapler & Reloads received FDA 510(k) clearance on 2020-12-14, under approval number K202467.

What company makes Disposable Powered Articulating Endoscopic Linear Cutter Stapler & Reloads?

Disposable Powered Articulating Endoscopic Linear Cutter Stapler & Reloads is manufactured by Fengh Medical Co., Ltd..

What is the FDA product code for Disposable Powered Articulating Endoscopic Linear Cutter Stapler & Reloads?

The FDA product code for Disposable Powered Articulating Endoscopic Linear Cutter Stapler & Reloads is GDW.

Related Clinical Trials

Other Devices by Fengh 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.