FDA 510(k) Applications Submitted by LUMENIS

FDA 510(k) Number Submission Date Device Name Applicant
K100415 02/16/2010 ACUPULSE 30/40 ST CO2 LASER SYSTEM AND ACUPULSE 40WG CO2 LASER SYSTEM LUMENIS
K030527 02/19/2003 LUMENIS FAMILY OF IPL AND COMBINATION IPL/ND:YAG SYSTEMS LUMENIS
K020591 02/22/2002 BCLEAR LUMENIS
K011197 04/19/2001 DERMACLEAR UV-B PHOTOTHERAPY SYSTEM LUMENIS
K011703 06/01/2001 LUMENIS VERSAPULSE POWERSUITE HOLMIUM (HO:YAG) AND DUAL WAVELENGTH (HO:YAG/ND:YAG) SURGICAL LASERS AND DELIVERY DEVICES LUMENIS


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