FDA 510(k) Applications Submitted by BRIAN KANERVIKO

FDA 510(k) Number Submission Date Device Name Applicant
K053350 12/02/2005 MODIFICATION TO CODMAN HAKIM SHUNT SYSTEMS Codman & Shurtleff, Inc.
K031213 04/17/2003 AQUASENS FLUID MONITORING SYSTEM DAVOL, INC.
K111751 06/22/2011 VERSAPOINT II BIPOLAR ELECTROSURGERY GENERATOR, VERSAPOINT II 44MM ANGLED LOOP ELECTRODE, VERSAPOINT II FOOTSWITCH, VERS ETHICON, INC.
K022350 07/19/2002 BARD CRURASOFT PATCH, MODELS 0116003 & 0116001 C.R. BARD, INC.
K024008 12/04/2002 SMALL BARD VENTRALEX PATCH C.R. BARD, INC.


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