The Karl Storz Mini 9000 Solid State Ccd Video Cam

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K881014 ↗

FDA Product Code

FWF

Device Class

Class I

Regulation

21 CFR Part 878.4160

Advisory Committee

General, Plastic Surgery

FDA Decision

SESE Substantially Equivalent

• KARL STORZ Laryngoscopes and Accessories

  Class II

  FDA 510(k) K252624 Active Cleared 15 May 2026

• Ksea Dion-Gracia Set

  Class II

  FDA 510(k) K010785 Active Cleared 21 Aug 2001

• Karl Storz Slotted Whisker Arthroscopic Blade

  Class II

  FDA 510(k) K963029 Active Cleared 27 Nov 1996

• Storz SLX-F2 Storm Touch

  Class II

  FDA 510(k) K070579 Active Cleared 30 Aug 2007

• Karl Storz Micro-Instrument for Cochlear Implantation

  Class I

  FDA 510(k) K946332 Active Cleared 5 Jun 1995

• Flexible Video-Uretero-Renoscope System Open recall

  Class II

  FDA 510(k) K131369 Active Cleared 26 Nov 2013

See all devices from Karl Storz Endoscopy-America, Inc. →