Advantage-Strand/Advantage-Load Brachytherapy Kit

FDA 510(k) K113210 · Isoaid, LLC

Substantially Equivalent

510(k) numberK113210

Submission

Device name
Advantage-Strand/Advantage-Load Brachytherapy Kit
Applicant
Isoaid, LLC
Port Richey, FL, US
Received
November 1, 2011
Decision date
August 10, 2012
Decision
Substantially Equivalent (SESE)
Type
Traditional 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

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More from Isoray Medical, Inc.

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K242818IsoSphereKXK · Traditional 07/15/2025SE
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K091117Advantage-Strand/ Advantage-Load Brachytherapy Kit, Model IaslbkaKXK · Traditional 09/15/2009SE
K033770Isoaid Advantage PD-103, Model IAPD-103AKXK · Traditional 04/08/2004SE
K011205Isoaid Iodine Brachtherapy Seeds, Model Advantage I-125KXK · Traditional 07/10/2001SE

Questions and answers

When was Advantage-Strand/Advantage-Load Brachytherapy Kit cleared by the FDA?

Advantage-Strand/Advantage-Load Brachytherapy Kit (K113210) received a 510(k) decision of Substantially Equivalent on August 10, 2012, 283 days after the submission was received.

What is the product code of K113210?

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