Reganes Radionuclide Seed Magazine

No FDA recalls on record, checked 9 Oct 2026.

510(k) Number

K972554 ↗

FDA Product Code

IWJ

Device Class

Class I

Regulation

21 CFR Part 892.5650

Advisory Committee

Radiology

FDA Decision

SESE Substantially Equivalent

• Aldrete Epidural Needle Without Introducer

  Class II

  FDA 510(k) K972595 Active Cleared 20 May 1998

• Avid-Nit Plastic Hub Lutz Epidural Needle, Model RP2035L, Avid-Nit Metal Hub Lutz Epidural Needle, Model RM2035L

  Class II

  FDA 510(k) K013231 Active Cleared 3 Dec 2001

• N.I.T., Inc. Needle Guiding Template

  Class I

  FDA 510(k) K973638 Active Cleared 23 Dec 1997

• Avid-Nit Nerve Stimulation Needles

  Class II

  FDA 510(k) K014246 Active Cleared 16 Jul 2002

• N.I.T., Inc. Radionuclide Seed Applicator, Model SA-1000

  Class I

  FDA 510(k) K973037 Active Cleared 27 Jan 1998

• N, I.T., Inc. Automatic Cutting Biopsy Needle

  Class II

  FDA 510(k) K983218 Active Cleared 6 Nov 1998

See all devices from Avid N.I.T., Inc. →