FDA 510(k) Applications Submitted by LEVO USA

FDA 510(k) Number Submission Date Device Name Applicant
K971873 05/20/1997 LEVO ACTIVE-EASY LAE LEVO USA
K963816 09/23/1996 LEVO COMPACT LC LEVO USA
K963817 09/23/1996 LEVO MOBIL LCM LEVO USA
K973951 10/16/1997 LEVO COMPACT-EASY LCE LEVO USA


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