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FDA 510(k) Applications Submitted by BREMED ITALIA, S.R.L.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K970542
02/12/1997
MASTER NEB II
BREMED ITALIA, S.R.L.
K982043
06/10/1998
BRENEB
BREMED ITALIA, S.R.L.
K974379
11/20/1997
ULTRANEB
BREMED ITALIA, S.R.L.
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