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FDA 510(k) Applications Submitted by THOMAS 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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