Medical Device Manufacturer · US , Minneapolis , MN

Clarus Medical Systems, Inc. - FDA 510(k) Cleared Devices

22 submissions · 20 cleared · Since 1992

Total

Cleared

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

1-12 of 22

Cleared Aug 18, 1998

CLARUS ENDOSCOPIC DISCECTOMY SYSTEM SITETRAC MODEL 6000

K980588 · GAD

General & Plastic Surgery · 182d

CLARUS MODEL 2127-900 SERIES ENDOSCOPE ADATER (2127-900 SERIES)

K971584 · OCV

Gastroenterology & Urology · 23d

Cleared May 20, 1997

CLARUS MODEL 5197 SIGHTLITE

K971455 · FTI

Gastroenterology & Urology · 29d

Cleared Dec 24, 1996

CLARUS NEUROPEN ENDOSCOPIC PLACEMENT KIT MODEL 2125-XXX

K960915 · GWG

Neurology · 293d

Cleared Sep 11, 1996

CLARUS MURPHYPEN ENDOSCOPE(2127-XXX)

K962255 · EOB

Ear, Nose, Throat · 91d

Cleared Feb 06, 1996

CLARUS SPINEPEN MODEL 2126

NEURO CHANNEL ENDOSCOPE MODEL 2232

K945633 · GWG

Neurology · 307d

Cleared Jul 14, 1995

CLARUS PHOENIX NEURO ENDOSCOPE MODEL 2160

K945296 · GWG

Neurology · 256d

Cleared Apr 25, 1995

CLARUS PHOENIX ENDOSCOPE

K940144 · HRX

Orthopedic · 469d

Cleared Apr 25, 1995

CLARUS NEURO ENDOSCOPE (MODEL 2230)

K941188 · HRX

Orthopedic · 407d

Clarus Medical Systems, Inc. - FDA 510(k) Cleared Devices

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