Cook Injection Needle

FDA 510(k) K022484 · Cook Urological, Inc.

Substantially Equivalent

510(k) numberK022484

Submission

Device name
Cook Injection Needle
Applicant
Cook Urological, Inc.
Spencer, IN, US
Received
July 29, 2002
Decision date
October 25, 2002
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
FBK – Endoscopic Injection Needle, Gastroenterology-Urology
Device class
Class II (moderate risk)
Regulation
21 CFR 876.1500
Specialty
Gastroenterology, Urology

inserted through endoscope for injection of a solution, gas, or implantable materials into gi or gu tissue.

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K082939Cook Fetal Membrane Manipulator, Model -FMM-122400KNA · Traditional 09/03/2009SE
K082066Tao Brush I.U.M.C. Endometrial SamplerHFE · Traditional 11/07/2008SE
K082536Cook Wire GuidesOCY · Traditional 10/27/2008SE
K082319Injekt Filiform Injection NeedleFBK · Traditional 09/25/2008SE
K080525Cook Odyssey Holmium Laser System, Model 30WGEX · Traditional 04/17/2008SE
K073496Optilite Holmium Laser FibersGEX · Traditional 01/23/2008SE
K072521Cook Fiber Optic Bundle and Flexor Deflecting Access SheathFFS · Traditional 11/20/2007SE
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Questions and answers

When was Cook Injection Needle cleared by the FDA?

Cook Injection Needle (K022484) received a 510(k) decision of Substantially Equivalent on October 25, 2002, 88 days after the submission was received.

What is the product code of K022484?

The FDA product code is FBK – Endoscopic Injection Needle, Gastroenterology-Urology, a Class II (moderate risk) device regulated under 21 CFR 876.1500.