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U.S. Department of Health and Human Services

510(k) Premarket Notification
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21 to 30 of 63 Results
ProductCode: GEX Applicant: LUMENIS Decision Date To: 02/10/2016
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vision one laser system LUMENIS INC. K111213 07/25/2011
acupulse 30/40 st co2 laser system and acupulse 40wg co2 laser system LUMENIS K100415 04/21/2010
fiberlase c02 laser waveguide LUMENIS, LTD. K100384 04/12/2010
versapulse model p20 laser system LUMENIS, INC. K100228 02/24/2010
lume 2 system, model ga0005000 LUMENIS, LTD. K083733 05/04/2009
acupulse 30 and 40 carbon dioxide laser system LUMENIS, INC. K082809 12/18/2008
selecta family of ophithalmic laser systems LUMENIS, INC. K081704 09/11/2008
lumenis one family of systems; lumenis one. LUMENIS LTD. K060448 07/06/2006
lightsheer duet laser system LUMENIS, INC. K053628 04/07/2006
family of selecta laser systems including selecta 1064, selecta slt, selecta duet, selecta duo, selecta trio LUMENIS, INC. K060338 03/09/2006
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