Karl Storz Imaging, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Karl Storz Imaging, Inc. - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Karl Storz Imaging, Inc. has 10 FDA 510(k) cleared medical devices. Based in Goleta, US.
Historical record: 10 cleared submissions from 1995 to 2001. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Karl Storz Imaging, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Karl Storz Imaging, Inc.
10 devices
Cleared
Apr 27, 2001
KSI'S NEW CAMERA ARCHITECTURE (NCA) VIDEO IMAGING SYSTEM
Gastroenterology & Urology
185d
Cleared
Jul 17, 2000
KARL STORZ 3D VIDEO SYSTEM
General & Plastic Surgery
80d
Cleared
Feb 04, 2000
KARL STORZ AUTOCLAVABLE CAMERA HEAD
Gastroenterology & Urology
63d
Cleared
Jun 01, 1999
KARL STORZ DIRECT COUPLED INTERFACE (DCI 5) CAMERA SYSTEM
General & Plastic Surgery
133d
Cleared
Jan 30, 1998
KARL STORZ ENDOVISION XL ENDOSCOPIC CAMERA SYSTEM
General & Plastic Surgery
70d
Cleared
Nov 24, 1997
KARL STORZ DIRECT COUPLED CAMERA HEAD
Gastroenterology & Urology
87d
Cleared
Oct 22, 1996
OPTRONICS EPIC COLOR TELEVISION CAMERA SYSTEM (S97340)
Ophthalmic
60d
Cleared
May 24, 1995
KARL STORZ ENDOVISION TRICAM, MODEL 20221101 (20221001, PAL FORMAT) COLOR...
General & Plastic Surgery
86d
Cleared
May 11, 1995
KARL STORZ ENDOVISION DIGIVIDEO (DIGITAL IMAGE PROCESSOR) ACCESSORY FOR COLOR...
Gastroenterology & Urology
70d
Cleared
May 11, 1995
KARL STORZ ENDOVISION TWINVIDEO (DIGITAL PICTURE-IN-PICTURE PROCESSOR)...
Gastroenterology & Urology
70d