Ksea Culdocentesis Set

No FDA recalls on record, checked 11 Oct 2026.

510(k) Number

K962881 ↗

FDA Product Code

HEW

Device Class

Class II

Regulation

21 CFR Part 884.1640

Advisory Committee

Obstetrics/Gynecology

FDA Decision

SESE Substantially Equivalent

• Ksea Gaab Neuroendoscope and Chavantes-Zaamorano Neuroendoscope Sets

  Class II

  FDA 510(k) K982837 Active Cleared 6 Nov 1998

• Ksea Quadro Switch

  Class II

  FDA 510(k) K021776 Active Cleared 15 Aug 2002

• Autocon II 200 Electrosurgical Generator

  Class II

  FDA 510(k) K023924 Active Cleared 21 Feb 2003

• Ksea Plastic Trocars

  Class II

  FDA 510(k) K974366 Active Cleared 8 Jan 1998

• Hand Extractor Hector

  Class II

  FDA 510(k) K953109 Active Cleared 25 Aug 1995

• Mvm 7.5 French Flexible Hysteroscope

  Class II

  FDA 510(k) K990411 Active Cleared 11 May 1999

See all devices from Karl Storz Endoscopy →