FDA 510(k) Applications Submitted by TOM BARTHEL
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| 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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