Laser Optik Systeme GmbH & Co. KG is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Laser Optik Systeme GmbH & Co. KG - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Laser Optik Systeme GmbH & Co. KG has 7 FDA 510(k) cleared medical devices. Based in Germany, DE.
Historical record: 7 cleared submissions from 1994 to 1999. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Laser Optik Systeme GmbH & Co. KG Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Laser Optik Systeme GmbH & Co. KG
7 devices
Cleared
Sep 14, 1999
XENON LIGHT SOURCE PES 1
Gastroenterology & Urology
47d
Cleared
Jul 30, 1997
STANDARD ENDOSCOPE
General & Plastic Surgery
58d
Cleared
May 14, 1996
PORTABLE ENDOSCOPY SYSTEM
Gastroenterology & Urology
455d
Cleared
Feb 08, 1996
LOS 3D VISION 100
General & Plastic Surgery
220d
Cleared
Jul 27, 1995
COLD LIGHT SOURCE LOS XL-A 100
Gastroenterology & Urology
87d
Cleared
Jul 10, 1995
COLD LIGHT SOURCE LOS 150
Ear, Nose, Throat
81d
Cleared
Apr 11, 1994
LOS 3D VISION 100
General & Plastic Surgery
411d