Disposable Hemostatic Clips

FDA 510(k) K232969 · Ningbo Xinwell Medical Technology Co., Ltd.

Substantially Equivalent

510(k) numberK232969

Submission

Device name
Disposable Hemostatic Clips
Applicant
Ningbo Xinwell Medical Technology Co., Ltd.
Ningbo Cixi, CN
Received
September 21, 2023
Decision date
June 7, 2024
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
PKL – Hemostatic Metal Clip For The Gi Tract
Device class
Class II (moderate risk)
Regulation
21 CFR 876.4400
Specialty
Gastroenterology, Urology
Implant
Yes
Life-sustaining
Yes

Clip placement within the gastrointestinal (GI) tract for the purpose of endoscopic marking, hemostasis for mucosal/sub-mucosal defects, bleeding ulcers, arteries, polyps, diverticula in the colon, prophylactic clipping, anchoring feeding tubes, supplemental closure method of luminal perforations.

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Questions and answers

When was Disposable Hemostatic Clips cleared by the FDA?

Disposable Hemostatic Clips (K232969) received a 510(k) decision of Substantially Equivalent on June 7, 2024, 260 days after the submission was received.

What is the product code of K232969?

The FDA product code is PKL – Hemostatic Metal Clip For The Gi Tract, a Class II (moderate risk) device regulated under 21 CFR 876.4400.