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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