HX-5/6-1 Endoscopic Clipping Device, Endoscopic Clips

FDA 510(k) K990687 · Olympus Optical, Co.

Substantially Equivalent

510(k) numberK990687

Submission

Device name
HX-5/6-1 Endoscopic Clipping Device, Endoscopic Clips
Applicant
Olympus Optical, Co.
Melville, NY, US
Received
March 1, 1999
Decision date
March 26, 1999
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 HX-5/6-1 Endoscopic Clipping Device, Endoscopic Clips cleared by the FDA?

HX-5/6-1 Endoscopic Clipping Device, Endoscopic Clips (K990687) received a 510(k) decision of Substantially Equivalent on March 26, 1999, 25 days after the submission was received.

What is the product code of K990687?

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.