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. |
|
|