Needle Technologies Seed Implant Needle

FDA 510(k) K921886 · Needle Technologies, Inc.

Substantially Equivalent

510(k) numberK921886

Submission

Device name
Needle Technologies Seed Implant Needle
Applicant
Needle Technologies, Inc.
Palm Harbor, FL, US
Received
April 21, 1992
Decision date
October 5, 1992
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

Other 510(k)s with product code IWJ

510(k)DeviceApplicantDecision
K010166Imagyn Isosleeve / Isostar Needle SystemIWJ · Traditional Imagyn Medical Technologies, Inc.12/03/2001SE
K980997PGK Device (Modified)IWJ · Traditional Pgk, Inc.09/28/1998SE
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

Questions and answers

When was Needle Technologies Seed Implant Needle cleared by the FDA?

Needle Technologies Seed Implant Needle (K921886) received a 510(k) decision of Substantially Equivalent on October 5, 1992, 167 days after the submission was received.

What is the product code of K921886?

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