PADLOCK CLIP EFTR Kit (00713229)

FDA 510(k) K250842 · STERIS Corporation

Substantially Equivalent

510(k) numberK250842

Submission

Device name
PADLOCK CLIP EFTR Kit (00713229)
Applicant
STERIS Corporation
Mentor, OH, US
Received
March 20, 2025
Decision date
April 18, 2025
Decision
Substantially Equivalent (SESE)
Type
Special 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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K250229Dual Action Tissue Closure DevicePKL · Traditional Micro-Tech (Nanjing) Co., Ltd.09/08/2025SE
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K241005Haemostasis ClipsPKL · Traditional Jiangxi Zhuoruihua Medical Instrument Co., Ltd.01/02/2025SE
K240274PADLOCK CLIP EFTR Kit (00713229)PKL · Traditional STERIS Corporation09/17/2024SE

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Questions and answers

When was PADLOCK CLIP EFTR Kit (00713229) cleared by the FDA?

PADLOCK CLIP EFTR Kit (00713229) (K250842) received a 510(k) decision of Substantially Equivalent on April 18, 2025, 29 days after the submission was received.

What is the product code of K250842?

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.