FDA 510(k) Applications Submitted by THOMAS C HAUCK

FDA 510(k) Number Submission Date Device Name Applicant
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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