FDA 510(k) Applications Submitted by MICHAEL NOEL KIERNAN

FDA 510(k) Number Submission Date Device Name Applicant
K000811 03/13/2000 NLITE SYSTEM, SLS MODEL NUMBER A00-1025 SLS BIOPHILE LTD.
K071883 07/09/2007 IPULSE, QUADRA Q4 PLATINUM SERIES, MODEL(S) 1200+SERIES 2, 1300 SERIES 2, Q4 SERIES 2 CYDEN LIMITED
K083748 12/17/2008 IPULSE, MODEL: I150 CYDEN LIMITED
K040156 01/23/2004 IFL PROFESSIONAL SYSTEM, MODEL C100 CYDEN LIMITED
K050165 01/25/2005 MODIFICATION TO IFL PROFESSIONAL SYSTEM, MODEL C100 CYDEN LIMITED


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