FDA 510(k) Applications Submitted by LIGHT AGE, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K110370 02/08/2011 Q-CLEAR LIGHT AGE, INC.
K091625 06/03/2009 EPICARE-DUO LASER SYSTEM LIGHT AGE, INC.
K113115 10/21/2011 EPICARE YAG LIGHT AGE, INC.
K980131 01/15/1998 ALEX TA2 ERASER LIGHT AGE, INC.
K983977 11/09/1998 LIGHT AGE EPICARE ALEXANDRITE LASER LIGHT AGE, INC.
K033259 10/09/2003 LIGHT AGE Q-CLEAR LASER, MODEL 701-1101 LIGHT AGE, INC.
K032991 09/25/2003 LIGHT AGE EPICARE ALEXANDRITE LASER, MODELS 501-1H, 501-SP, 501-LP AND 501-LPX LIGHT AGE, INC.


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