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Clarus Medical Systems, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
22
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K980588CLARUS ENDOSCOPIC DISCECTOMY SYSTEM SITETRAC MODEL 6000August 18, 1998
K974579PERCSCOPE MODEL 2600February 18, 1998
K971584CLARUS MODEL 2127-900 SERIES ENDOSCOPE ADATER (2127-900 SERIES)May 23, 1997
K971455CLARUS MODEL 5197 SIGHTLITEMay 20, 1997
K960915CLARUS NEUROPEN ENDOSCOPIC PLACEMENT KIT MODEL 2125-XXXDecember 24, 1996
K962255CLARUS MURPHYPEN ENDOSCOPE(2127-XXX)September 11, 1996
K955598CLARUS SPINEPEN MODEL 2126February 6, 1996
K953685INSTRUMENT SCOPEOctober 12, 1995
K945633NEURO CHANNEL ENDOSCOPE MODEL 2232September 19, 1995
K945296CLARUS PHOENIX NEURO ENDOSCOPE MODEL 2160July 14, 1995
K941188CLARUS NEURO ENDOSCOPE (MODEL 2230)April 25, 1995
K940144CLARUS PHOENIX ENDOSCOPEApril 25, 1995
K942413CLARUS ENDOSCOPIC NEUROLOGICAL TISSUE ELEVATORNovember 22, 1994
K942249CLARUS NEUROPEN MODEL 2120November 4, 1994
K923514CLARUS SERIES 2100 ENDOSCOPEJanuary 7, 1994
K932259CLARUS MODEL 2240 SEMI-RIGID OTOSCOPEDecember 15, 1993
K925741CLARUS ENDOSCOPIC HOOK KNIFEAugust 24, 1993
K925742CLARUS CHOLANGIOGRAM CATHETER KITJune 1, 1993
K926048CLARUS ENDOSCOPIC BALL PROBEApril 7, 1993
K924554CLARUS SERIRS 2200 SEMI-RIGID ENDOSCOPEFebruary 25, 1993