FDA 510(k) Applications Submitted by CLARUS MEDICAL, LLC.

FDA 510(k) Number Submission Date Device Name Applicant
K082038 07/17/2008 CLARUS VIDEO AIRWAY ENDOSCOPE, MODELS 30000-V AND 30003-V CLARUS MEDICAL, LLC.
K040424 02/18/2004 LASER ENDOSCOPIC DECOMPRESSION KIT, MODEL 1100, AND PERCUTANEOUS DISCECTOMY KIT, MODEL 1120 CLARUS MEDICAL, LLC.
K040919 04/08/2004 NUCLEOTOME PROBE SET, MODEL 21200 CLARUS MEDICAL, LLC.
K011454 05/11/2001 SPINE SCOPE, MODEL 2180 CLARUS MEDICAL, LLC.
K021848 06/05/2002 CLARUS STRAIGHT FIRING LASER FIBER; CLARUS SIDE FIRING LASER FIBER; MODELS 1150, 1160 CLARUS MEDICAL, LLC.
K022610 08/06/2002 CLARUS STRAIGHT FIRING LASER FIBER, MODEL 1150, CLARUS SIDE FIRING LASER FIBER, MODEL 1160 CLARUS MEDICAL, LLC.


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