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FDA 510(k) Applications Submitted by THOMAS RAEBER
FDA 510(k) Number
Submission Date
Device Name
Applicant
K030893
03/21/2003
LEVO COMBI
LEVO AG
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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