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Lumenis

FDA 510(k) & PMA Approved Devices — 5 products

Total Devices5

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K100415	ACUPULSE 30/40 ST CO2 LASER SYSTEM AND ACUPULSE 40WG CO2 LASER SYSTEM	GEX	2010-04-21	View
510(k)	K030527	LUMENIS FAMILY OF IPL AND COMBINATION IPL/ND:YAG SYSTEMS	GEX	2003-05-20	View
510(k)	K020591	BCLEAR	FTC	2002-05-16	View
510(k)	K011197	DERMACLEAR UV-B PHOTOTHERAPY SYSTEM	FTC	2001-12-14	View
510(k)	K011703	LUMENIS VERSAPULSE POWERSUITE HOLMIUM (HO:YAG) AND DUAL WAVELENGTH (HO:YAG/ND:YAG) SURGICAL LASERS AND DELIVERY DEVICES	GEX	2001-08-29	View

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