Ez-Pak (Ez-Pak Is a Trademark of Ibt S.A.)

Q: What is the product code of K041702?

The FDA product code is KXK – Source, Brachytherapy, Radionuclide, a Class II (moderate risk) device regulated under 21 CFR 892.5730.

FDA 510(k) K041702 · Ibt SA

Substantially Equivalent

510(k) numberK041702

Submission

Device name: Ez-Pak (Ez-Pak Is a Trademark of Ibt S.A.)
Applicant: Ibt SA
Norcross, GA, US
Received: June 22, 2004
Decision date: July 16, 2004
Decision: Substantially Equivalent (SESE)
Type: Special 510(k)
Summary: 510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code: KXK – Source, Brachytherapy, Radionuclide
Device class: Class II (moderate risk)
Regulation: 21 CFR 892.5730
Specialty: Radiology
Implant: Yes

Other 510(k)s with product code KXK

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K252296	OncoPatchKXK · Traditional	Oncopatch, Inc.	12/05/2025SE
K242818	IsoSphereKXK · Traditional	Isoaid, LLC	07/15/2025SE
K223465	RadianceTx Radionuclide Brachytherapy SourceKXK · Traditional	Radiance Therapeutics, Inc.	01/11/2023SE
K221539	GammaTileKXK · Traditional	Gt Medical Technologies	11/09/2022SE
K202267	Sirius MRI Markers, Cs-131 Preloaded Strands with Sirius MRI Markers in 18 Gauge NeedlesKXK · Traditional	Isoray Medical, Inc.	12/31/2020SE
K193602	LV Liberty Vision Model 1 90Yttrium Brachytherapy SourceKXK · Special	Lv Liberty Vision Corporation	05/29/2020SE
K190839	GammaTileKXK · Traditional	Gt Medical Technologies	01/23/2020SE
K191324	CivaDermKXK · Traditional	Civatech Oncology, Inc.	09/20/2019SE
K190296	GammaTileKXK · Special	Gt Medical Technologies	03/13/2019SE
K180515	GammaTileKXK · Traditional	Isoray Medical, Inc.	07/06/2018SE

More from Isoray Medical, Inc.

510(k)	Device	Decision
K043336	Optistrand, Model 1032SKXK · Traditional	01/21/2005SE
K011155	Interstrand 125 & Interstrand 103, Model Numbers 1251S and 1031SKXK · Abbreviated	07/12/2001SE

Questions and answers

When was Ez-Pak (Ez-Pak Is a Trademark of Ibt S.A.) cleared by the FDA?

Ez-Pak (Ez-Pak Is a Trademark of Ibt S.A.) (K041702) received a 510(k) decision of Substantially Equivalent on July 16, 2004, 24 days after the submission was received.

What is the product code of K041702?

The FDA product code is KXK – Source, Brachytherapy, Radionuclide, a Class II (moderate risk) device regulated under 21 CFR 892.5730.