Morganstern Prostate Stabilization and Seeding Kit

FDA 510(k) K944522 · Medical Device Technologies, Inc.

Substantially Equivalent

510(k) numberK944522

Submission

Device name
Morganstern Prostate Stabilization and Seeding Kit
Applicant
Medical Device Technologies, Inc.
Gainsville, FL, US
Received
September 16, 1994
Decision date
February 24, 1995
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
IWJ – System, Applicator, Radionuclide, Manual
Device class
Class I (low risk)
Regulation
21 CFR 892.5650
Specialty
Radiology

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K972554Reganes Radionuclide Seed MagazineIWJ · Traditional Avid N.I.T., Inc.02/17/1998SE
K973037N.I.T., Inc. Radionuclide Seed Applicator, Model SA-1000IWJ · Traditional Avid N.I.T., Inc.01/27/1998SE
K974118Worldwide Medical Technologies Seed Implant Needle SetIWJ · Traditional Worldwide Medical Technologies, LLC01/23/1998SE
K973786Northwest Radiation Therapy Products, Precision Stepper and GuideIWJ · Traditional Nw Radiation Therapy Products01/02/1998SE
K973638N.I.T., Inc. Needle Guiding TemplateIWJ · Traditional Avid N.I.T., Inc.12/23/1997SE
K973184Prostate Seeding NeedleIWJ · Traditional Promex, Inc.11/21/1997SE
K963743Manan Prostate Uni-LockIWJ · Traditional Manan Medical Products, Inc.12/06/1996SE
K951052Weeks ApplicatorIWJ · Traditional Duke University Medical Center08/22/1996SE

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Questions and answers

When was Morganstern Prostate Stabilization and Seeding Kit cleared by the FDA?

Morganstern Prostate Stabilization and Seeding Kit (K944522) received a 510(k) decision of Substantially Equivalent on February 24, 1995, 161 days after the submission was received.

What is the product code of K944522?

The FDA product code is IWJ – System, Applicator, Radionuclide, Manual, a Class I (low risk) device regulated under 21 CFR 892.5650.