FDA 510(k) Applications Submitted by ROLENCE ENTERPRISE CO. LTD.

FDA 510(k) Number Submission Date Device Name Applicant
K960351 01/25/1996 Q-LUX LIGHT CURE UNIT ROLENCE ENTERPRISE CO. LTD.
K960364 01/25/1996 CU-200 LIGHT CURE UNIT ROLENCE ENTERPRISE CO. LTD.
K980792 03/02/1998 CU-100A LIGHT CURE UNIT ROLENCE ENTERPRISE CO. LTD.
K980793 03/02/1998 Q-LUXPRO V/Q-LUXPRO II LIGHT CURE UNIT ROLENCE ENTERPRISE CO. LTD.
K991863 06/01/1999 CUTE-LITE I LIGHT CURE UNIT ROLENCE ENTERPRISE CO. LTD.
K991865 06/01/1999 Q-LITE 75 LIGHT CURE UNIT ROLENCE ENTERPRISE CO. LTD.
K001719 06/05/2000 Q-LUX PLASMA 100 LIGHT CURE UNIT ROLENCE ENTERPRISE CO. LTD.


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