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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