FDA 510(k) Applications Submitted by LISA LACROIX

FDA 510(k) Number Submission Date Device Name Applicant
K081324 05/12/2008 CANDELA FAMILY OF Q-SWITCHED ALEXANDRITE LASERS CANDELA CORP.
K073534 12/17/2007 CANDELA FAMILY OF Q-SWITCHED ALEXANDRITE LASER (ALEXLAZR) SYSTEMS CANDELA CORP.


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