Clarus Medical Systems, Inc.
FDA 510(k) medical device clearances.
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.