Henschke Afterloading Applicator

FDA 510(k) K871217 · Mick Radio-Nuclear Instruments, Inc.

Substantially Equivalent

510(k) numberK871217

Submission

Device name
Henschke Afterloading Applicator
Applicant
Mick Radio-Nuclear Instruments, Inc.
Bronx, NY, US
Received
March 26, 1987
Decision date
July 16, 1987
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

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 Henschke Afterloading Applicator cleared by the FDA?

Henschke Afterloading Applicator (K871217) received a 510(k) decision of Substantially Equivalent on July 16, 1987, 112 days after the submission was received.

What is the product code of K871217?

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