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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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