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FDA 510(k) Applications Submitted by MICHELLE DEETON
FDA 510(k) Number
Submission Date
Device Name
Applicant
K990947
03/22/1999
MODIFIED VERSAPULSE SELECT SINGLE WAVELENGTH, HO: YAG AND DUAL WAVELENGTH, HO: YAG/ND: YAG SURGICAL LASERS AND DELIVERY
LUMENIS, INC.
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