Clarus Medical Systems, Inc. is one of 15035 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Clarus Medical Systems, Inc. - FDA 510(k) Cleared Devices
Recent clearances: CLARUS ENDOSCOPIC DISCECTOMY SYSTEM SITETRAC MODEL 6000, PERCSCOPE MODEL 2600, CLARUS MODEL 2127-900 SERIES ENDOSCOPE ADATER (2127-900 SERIES)
22
Total
20
Cleared
0
Denied
Clarus Medical Systems, Inc. has 20 FDA 510(k) cleared medical devices. Based in Minneapolis, US.
Historical record: 20 cleared submissions from 1992 to 1998.
Browse the FDA 510(k) cleared devices submitted by Clarus Medical Systems, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Clarus Medical Systems, Inc.
22 devices
Cleared
Aug 18, 1998
CLARUS ENDOSCOPIC DISCECTOMY SYSTEM SITETRAC MODEL 6000
General & Plastic Surgery
182d
Cleared
Feb 18, 1998
PERCSCOPE MODEL 2600
Orthopedic
72d
Cleared
May 23, 1997
CLARUS MODEL 2127-900 SERIES ENDOSCOPE ADATER (2127-900 SERIES)
Gastroenterology & Urology
23d
Cleared
May 20, 1997
CLARUS MODEL 5197 SIGHTLITE
Gastroenterology & Urology
29d
Cleared
Dec 24, 1996
CLARUS NEUROPEN ENDOSCOPIC PLACEMENT KIT MODEL 2125-XXX
Neurology
293d
Cleared
Sep 11, 1996
CLARUS MURPHYPEN ENDOSCOPE(2127-XXX)
Ear, Nose, Throat
91d
Cleared
Feb 06, 1996
CLARUS SPINEPEN MODEL 2126
Neurology
60d
Cleared
Oct 12, 1995
INSTRUMENT SCOPE
Neurology
66d
Cleared
Sep 19, 1995
NEURO CHANNEL ENDOSCOPE MODEL 2232
Neurology
307d
Cleared
Jul 14, 1995
CLARUS PHOENIX NEURO ENDOSCOPE MODEL 2160
Neurology
256d
Cleared
Apr 25, 1995
CLARUS PHOENIX ENDOSCOPE
Orthopedic
469d
Cleared
Apr 25, 1995
CLARUS NEURO ENDOSCOPE (MODEL 2230)
Orthopedic
407d