Headlamp HL2000.

No FDA recalls found in the data synced 9 Oct 2026.

510(k) Number

K994362 ↗

FDA Product Code

FSR

Device Class

Class II

Regulation

21 CFR Part 886.4335

Advisory Committee

Ophthalmic

FDA Decision

SESE Substantially Equivalent

• Ves 3001/2 Dual Output Video Illuminator

  Class II

  FDA 510(k) K981821 Active Cleared 29 Jul 1998

• Ves 3001-M Complete Video Endoscopic System

  Class I

  FDA 510(k) K982397 Active Cleared 10 Sep 1998

• Angiolaz Angioscope Catheter

  Class II

  FDA 510(k) K913129 Active Cleared 27 Dec 1991

• Ves 1501-M

  Class I

  FDA 510(k) K982409 Active Cleared 21 Aug 1998

• 50 W Metal Halide Illuminator, Ves 0501.

  Class II

  FDA 510(k) K992447 Active Cleared 20 Oct 1999

• Ves 0281-M Complete Video Endoscopic Video System

  Class II

  FDA 510(k) K981827 Active Cleared 28 Jul 1998

See all devices from Angiolaz, Inc. →