Clarus Medical, LLC
FDA 510(k) medical device clearances.
Top product codes for Clarus Medical, LLC
Recent clearances by Clarus Medical, LLC
- K240535 — Digital ClarusScope System; Digital NeuroPEN System
- K223615 — Digital ClarusScope System, Digital NeuroPEN System
- K200925 — Clarus Peel-Away Introducer Sheath
- K082038 — CLARUS VIDEO AIRWAY ENDOSCOPE, MODELS 30000-V AND 30003-V
- K040919 — NUCLEOTOME PROBE SET, MODEL 21200
- K040424 — LASER ENDOSCOPIC DECOMPRESSION KIT, MODEL 1100, AND PERCUTANEOUS DISCECTOMY KIT, MODEL 1120
- K022610 — CLARUS STRAIGHT FIRING LASER FIBER, MODEL 1150, CLARUS SIDE FIRING LASER FIBER, MODEL 1160
- K021848 — CLARUS STRAIGHT FIRING LASER FIBER; CLARUS SIDE FIRING LASER FIBER; MODELS 1150, 1160
- K011454 — SPINE SCOPE, MODEL 2180
Data sourced from openFDA. This site is unofficial and independent of the FDA.