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FDA 510(k) Applications Submitted by AXIOM USA. INC
FDA 510(k) Number
Submission Date
Device Name
Applicant
K030622
02/27/2003
AXIOM BIOLASER LLLT SERIES-1
AXIOM USA. INC
K022602
08/06/2002
DRX3000
AXIOM USA. INC
K023160
09/23/2002
DRX5000
AXIOM USA. INC
K033015
09/26/2003
AXIOM BIOLASER LLLT SERIES-3
AXIOM USA. INC
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