Sl-100 Nd:yag Laser for Pulmonary Obstructions

No FDA recalls found in the data synced 11 Oct 2026.

510(k) Number

K871511 ↗

FDA Product Code

LLO

Device Class

Class II

Regulation

21 CFR Part 874.4500

Advisory Committee

Ear, Nose, Throat

FDA Decision

SESE Substantially Equivalent

• SL-100 Nd:YAG Laser for Urologic Surgery

  Class II

  FDA 510(k) K871516 Active Cleared 9 Jul 1987

• Sl-100 Nd:yag Laser for Gastrointestinal Bleeding

  Class II

  FDA 510(k) K871515 Active Cleared 9 Jul 1987

• Sl-100 Nd:yag Laser for Palliation of Gastro. Mali

  Class II

  FDA 510(k) K871513 Active Cleared 9 Jul 1987

• Lightforce Lf 20/30 980NM Surgical Diode Laser System

  Class II

  FDA 510(k) K041419 Active Cleared 26 Aug 2004

• Sl-100 Nd:yag Laser for Rectal Patho. & Hemorrhoid

  Class II

  FDA 510(k) K871514 Active Cleared 9 Jul 1987

• Sl-100 Nd:yag Laser for Gynecology Use

  Class II

  FDA 510(k) K871512 Active Cleared 8 Jul 1988