Aldrete Epidural Needle Without Introducer

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K972595 ↗

FDA Product Code

BSP

Device Class

Class II

Regulation

21 CFR Part 868.5150

Advisory Committee

Anesthesiology

FDA Decision

SESE Substantially Equivalent

• Reganes Radionuclide Seed Magazine

  Class I

  FDA 510(k) K972554 Active Cleared 17 Feb 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. →