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FDA 510(k) Applications Submitted by GEOFFREY D SWANK
FDA 510(k) Number
Submission Date
Device Name
Applicant
K062248
08/03/2006
AZURYT MODEL CTL 1401, CO2 SURGICAL LASER SYSTEM
NORTH AMERICAN CLINICAL LASERS, LTD.
K042439
09/09/2004
AZURYT MODEL CLT 1401, CO2 SURGICAL LASER SYSTEM
DIAMOND AGE SYSTEMS, INC.
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