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Sandstone Medical Technologies, LLC

FDA 510(k) & PMA Approved Devices — 11 products

Total Devices11

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K121162	POLARIS Q-SWITCH RUBY SYSTEM	GEX	2012-07-18	View
510(k)	K110897	CORTEX CO2 / ER:YAG LASER SYSTEM	GEX	2011-07-01	View
510(k)	K110502	TRIPLEX ER. YAG / ND: YAG SYSTEM	GEX	2011-04-27	View
510(k)	K110304	APEX ER. YAG / IPL SYSTEM	GEX	2011-04-08	View
510(k)	K100893	CHEVEUX DIODE LASER SYSTEM	GEX	2010-06-16	View
510(k)	K093793	LS-40 CO2 LASER SYSTEM MODEL LS-40	GEX	2010-02-18	View
510(k)	K082407	MODIFICATION TO ULTRALIGHT II ND: YAG LASER SYSTEM	GEX	2009-02-03	View
510(k)	K082101	LS FAMILY OF CO2 LASERS WITH SCANNING HANDPIECE	GEX	2008-11-05	View
510(k)	K081219	APOLLO MINI IPL SYSTEM	GEX	2008-06-30	View
510(k)	K041011	ULTRALIGHT II ND:YAG LASER SYSTEM	GEX	2004-12-14	View
510(k)	K040563	LS FAMILY OF CO2 LASERS INCLUDING: LS-15 LASER SYSTEM (15 WATT) AND LS-25 LASER SYSTEM (25 WATT)	GEX	2004-10-08	View

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