Laparoscopic Vessel Articulator

No FDA recalls on record, checked 11 Oct 2026.

510(k) Number

K911475 ↗

FDA Product Code

DWP

Device Class

Class II

Regulation

21 CFR Part 870.4475

Advisory Committee

Cardiovascular

FDA Decision

SESE Substantially Equivalent

• U.S. Endoscopy Pull Peg Kit & U.S. Endoscopy Guidewire Peg Kit

  Class II

  FDA 510(k) K955248 Active Cleared 21 May 1996

• Concentric Balloon Google

  Class II

  FDA 510(k) K112698 Active Cleared 18 May 2012

• Disposable Overtube

  Class II

  FDA 510(k) K040836 Active Cleared 10 Jun 2004

• Coaxial Needle

  Class II

  FDA 510(k) K971842 Active Cleared 20 Jun 1997

• Papillotome

  Class II

  FDA 510(k) K962346 Active Cleared 8 Aug 1996

• Biopsy Forceps, Electric

  Class II

  FDA 510(k) K925361 Active Cleared 29 Mar 1993

See all devices from United States Endoscopy Group, Inc. →