Jarit Surgical Instruments

• • Terminated Z-0886-2013 FDA Class II ·initiated 12 Feb 2013

  Addendum to the Instructions for Use. The addendum emphasizes the warnings and precautions already contained in the device's IFU and also provides additional warnings and precautions that are applicable to the use of electrosurgical equipment in health care facility environments.

510(k) Number

K932456 ↗

FDA Product Code

KNF

Device Class

Class II

Regulation

21 CFR Part 884.4160

Advisory Committee

Obstetrics/Gynecology

FDA Decision

SESE Substantially Equivalent

• Jarit Endoscopes, 600-600; 600-630; 600-650; 680

  Class II

  FDA 510(k) K931878 Active Cleared 19 Aug 1993

• Cope Lung Forceps #305-218

  Class I

  FDA 510(k) K771624 Active Cleared 6 Sep 1977

• Jarit Surgical Instruments

  Class II

  FDA 510(k) K931959 Active Cleared 5 Oct 1993

• Jarit Recommended Sinus Instruments

  Class II

  FDA 510(k) K944670 Active Cleared 2 Feb 1995

• Leiningeo Aortic Punch #310-395 & 397

  Class I

  FDA 510(k) K771625 Active Cleared 12 Sep 1977

• Jarit Hulka Uterine Tenaculum Forceps

  Class II

  FDA 510(k) K082349 Active Cleared 21 Nov 2008

See all devices from J. Jamner Surgical Instruments, Inc. →