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FDA 510(k) Applications Submitted by JOHN VADEN 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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