Light Sabre Spinal Access Device

No FDA recalls found in the data synced 22 Oct 2026.

510(k) Number

K071814 ↗

FDA Product Code

KNW

Device Class

Class II

Regulation

21 CFR Part 876.1075

Advisory Committee

Gastroenterology, Urology

FDA Decision

SESE Substantially Equivalent

• DRTS Image Intensifier Drape

  Class II

  FDA 510(k) K973073 Active Cleared 8 Oct 1997

• Sabresource Drape

  Class II

  FDA 510(k) K041846 Active Cleared 26 Aug 2004

• MR Fiber Optic Intubating Laryngoscope Handle, Standard, Model 310001

  Class I

  FDA 510(k) K062231 Active Cleared 31 Aug 2006

• Minrad Drts Light Saber Syringe

  Class II

  FDA 510(k) K981140 Active Cleared 25 Jun 1998

• MR Tested Fiber Optic Short Laryngoscope Handle, Model 310002

  Class I

  FDA 510(k) K041852 Active Cleared 15 Nov 2004

• Light Saber Aspiration Needle

  Class II

  FDA 510(k) K982018 Active Cleared 7 Aug 1998

See all devices from Minrad, Inc. →