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FDA 510(k) Applications Submitted by GLOBAL USA DISTRIBUTION, LLC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K082028
07/17/2008
LASERPEEL SOFT-MET MODIFIED ERBIUM LASER
GLOBAL USA DISTRIBUTION, LLC.
K082033
07/17/2008
NANNOLIGHT INTENSE PULSED LIGHT SYSTEM
GLOBAL USA DISTRIBUTION, LLC.
K083272
11/06/2008
SKINCLEAR Q-SWITCHED ND:YAG LASER
GLOBAL USA DISTRIBUTION, LLC.
K080697
03/12/2008
SKIN CLEAR SRVH LONG-PULSED ND: YAG LASER
GLOBAL USA DISTRIBUTION, LLC.
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