FDA 510(k) Applications Submitted by JOHN VANDEN HOEK

FDA 510(k) Number Submission Date Device Name Applicant
K962255 06/12/1996 CLARUS MURPHYPEN ENDOSCOPE(2127-XXX) CLARUS MEDICAL SYSTEMS, INC.
K955598 12/08/1995 CLARUS SPINEPEN MODEL 2126 CLARUS MEDICAL SYSTEMS, INC.
K960915 03/06/1996 CLARUS NEUROPEN ENDOSCOPIC PLACEMENT KIT MODEL 2125-XXX CLARUS MEDICAL SYSTEMS, INC.


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