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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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