Clarus Medical Systems, Inc.
Clarus Medical Systems, Inc. holds FDA 510(k) medical device clearances, first cleared 1992, most recent 1998.
Top product codes for Clarus Medical Systems, Inc.
Recent clearances by Clarus Medical Systems, Inc.
- K980588 — CLARUS ENDOSCOPIC DISCECTOMY SYSTEM SITETRAC MODEL 6000
- K974579 — PERCSCOPE MODEL 2600
- K971584 — CLARUS MODEL 2127-900 SERIES ENDOSCOPE ADATER (2127-900 SERIES)
- K971455 — CLARUS MODEL 5197 SIGHTLITE
- K960915 — CLARUS NEUROPEN ENDOSCOPIC PLACEMENT KIT MODEL 2125-XXX
- K962255 — CLARUS MURPHYPEN ENDOSCOPE(2127-XXX)
- K955598 — CLARUS SPINEPEN MODEL 2126
- K953685 — INSTRUMENT SCOPE
- K945633 — NEURO CHANNEL ENDOSCOPE MODEL 2232
- K945296 — CLARUS PHOENIX NEURO ENDOSCOPE MODEL 2160
- K940144 — CLARUS PHOENIX ENDOSCOPE
- K941188 — CLARUS NEURO ENDOSCOPE (MODEL 2230)
- K942413 — CLARUS ENDOSCOPIC NEUROLOGICAL TISSUE ELEVATOR
- K942249 — CLARUS NEUROPEN MODEL 2120
- K923514 — CLARUS SERIES 2100 ENDOSCOPE
- K932259 — CLARUS MODEL 2240 SEMI-RIGID OTOSCOPE
- K925741 — CLARUS ENDOSCOPIC HOOK KNIFE
- K925742 — CLARUS CHOLANGIOGRAM CATHETER KIT
- K926048 — CLARUS ENDOSCOPIC BALL PROBE
- K924554 — CLARUS SERIRS 2200 SEMI-RIGID ENDOSCOPE
- K915725 — CLARUS MODELS 1230 AND 1231 LAPARO-NEEDLE
- K922881 — CLARUS MODELS 1100, 1101, 1102, 1103 LASER DISC
Data sourced from openFDA. This site is unofficial and independent of the FDA.