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FDA 510(k) Applications Submitted by Owen Mumford USA, Inc.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K982275
06/29/1998
RAPPORT V.T.D.
Owen Mumford USA, Inc.
K993385
10/08/1999
AUTOJET 2 (NON-FIXED NEEDLE TYPE)
Owen Mumford USA, Inc.
K013362
10/10/2001
AUTOJECT 2
OWEN MUMFORD USA, INC.
K983974
11/09/1998
OWEN MUMFORD 3ML AUTOPEN
Owen Mumford USA, Inc.
K983994
11/09/1998
UNIFINE
Owen Mumford USA, Inc.
K971443
04/21/1997
RAPPORT V.T.D.
OWEN MUMFORD USA, INC.
K983045
09/01/1998
AMIELLE
Owen Mumford USA, Inc.
K973899
10/14/1997
UNIFINE PENTIPS
Owen Mumford USA, Inc.
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