5, 6, 7, 9, 10, 11, 12mm Blunt-Tip Trocar Obtur/Thread

No FDA recalls found in the data synced 10 Oct 2026.

510(k) Number

K934510 ↗

FDA Product Code

GCL

Device Class

Class II

Regulation

21 CFR Part 876.1500

Advisory Committee

Gastroenterology, Urology

FDA Decision

SESE Substantially Equivalent

• Hydro-Probe

  Class II

  FDA 510(k) K934157 Active Cleared 26 Jan 1994

• Sterile, Disposable Endoscopic Trumpet Valve

  Class II

  FDA 510(k) K934098 Active Cleared 16 Dec 1993

• Watts Rake with Leur Lock Port

  Class II

  FDA 510(k) K934153 Active Cleared 18 Mar 1994

• 5, 6, 7, 9, 10, 11&12mm Blunt-Tipped Trocar Obturators

  Class II

  FDA 510(k) K934511 Active Cleared 17 Feb 1994

• Phx Technologies Corp., Bowel Grasper Device

  Class II

  FDA 510(k) K934021 Active Cleared 17 Dec 1993

• Phx Technologies Corp. Bowel Grasper Device

  Class II

  FDA 510(k) K934026 Active Cleared 17 Dec 1993

See all devices from Phx Technologies Corp. →