Resolution Clip, Resolution 360 Clip, Resolution 360 ULTRA Clip

FDA 510(k) K222503 · Boston Scientific Corporation

Substantially Equivalent

510(k) numberK222503

Submission

Device name
Resolution Clip, Resolution 360 Clip, Resolution 360 ULTRA Clip
Applicant
Boston Scientific Corporation
Marlboro, MA, US
Received
August 18, 2022
Decision date
September 14, 2022
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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Questions and answers

When was Resolution Clip, Resolution 360 Clip, Resolution 360 ULTRA Clip cleared by the FDA?

Resolution Clip, Resolution 360 Clip, Resolution 360 ULTRA Clip (K222503) received a 510(k) decision of Substantially Equivalent on September 14, 2022, 27 days after the submission was received.

What is the product code of K222503?

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.