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FDA 510(k) Applications Submitted by INTERMEDIC ARFRAN, S.A.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K091323
05/05/2009
MODIFIED INTERMEDIC DIODE LASER 980NM SYSTEM (MULTIDIODE SST 200)
INTERMEDIC ARFRAN, S.A.
K053540
12/20/2005
INTERMEDIC DIODE LASER FAMILY 810NM AND 980NM (AND THE DELIVERY ACCESSORIES THAT ARE USED WITH THEM TO DELIVER LASER ENE
INTERMEDIC ARFRAN, S.A.
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