Rita Model 70 Electrosurgical Probe

• • Terminated Z-0753-2007 FDA Unclassified (pre-2012) ·initiated 3 Apr 2007

  The product may have a cracked tray which can compromise the sterility of the product.

510(k) Number

K983871 ↗

FDA Product Code

GEI

Device Class

Class II

Regulation

21 CFR Part 878.4400

Advisory Committee

General, Plastic Surgery

FDA Decision

SESE Substantially Equivalent

• Vortex Ez Vascular Access Port

  Class II

  FDA 510(k) K050176 Active Cleared 25 Feb 2005

• Omnipicc Pi

  Class II

  FDA 510(k) K051102 Active Cleared 23 Nov 2005

• Rita Rf Generator and Accessories, Model 500 Series

  Class II

  FDA 510(k) K983214 Active Cleared 27 Mar 2000

• Rita Model 1500X Electrosurgical Rf Generator

  Class II

  FDA 510(k) K031257 Active Cleared 2 May 2003

• Rita System

  Class II

  FDA 510(k) K021329 Active Cleared 9 Oct 2002

• Omnipicc P.I.

  Class II

  FDA 510(k) K062579 Active Cleared 28 Nov 2006

See all devices from Rita Medical Systems, Inc. →