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FDA 510(k) Applications Submitted by PHILLIP CHEON
FDA 510(k) Number
Submission Date
Device Name
Applicant
K083203
10/30/2008
HELIOS II Q-SWITCHED ND:YAG LASER SYSTEM
LASEROPTEK CO. LTD.
K083253
11/04/2008
LOTUS II PULSED ER: YAG LASER SYSTEM
LASEROPTEK CO. LTD.
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