Manan Prostate Seeding Needle

FDA 510(k) K902622 · Manan Medical Products, Inc.

Substantially Equivalent

510(k) numberK902622

Submission

Device name
Manan Prostate Seeding Needle
Applicant
Manan Medical Products, Inc.
Northbrook, IL, US
Received
June 14, 1990
Decision date
August 10, 1990
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

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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K052802Manan Bio-Cut Soft Tissue Biopsy NeedleKNW · Special 11/01/2005SE
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K983620Manan Spinal NeedlesBSP · Traditional 01/08/1999SE
K980536Epidural NeedleBSP · Traditional 07/31/1998SE
K981386Manan Blunt NeedleFPA · Traditional 06/29/1998SE
K980211MRI Chiba,Spinal,Breast Localization,Automatic Cutting NeedlesKNW · Traditional 02/06/1998SE
K974446Manan Automatic Cutting NeedleKNW · Traditional 01/08/1998SE
K962977MRI Compatible Biopsy NeedlesKNW · Traditional 10/09/1997SE
K963767Manan V.S. Access Needle/SetFGE · Traditional 05/16/1997SE
K961986Manan D BagEXF · Traditional 03/13/1997SE

Questions and answers

When was Manan Prostate Seeding Needle cleared by the FDA?

Manan Prostate Seeding Needle (K902622) received a 510(k) decision of Substantially Equivalent on August 10, 1990, 57 days after the submission was received.

What is the product code of K902622?

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