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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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