FDA 510(k) Applications Submitted by ROBERT E SHAW
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K000482 |
02/14/2000 |
MODIFICATION TO AUTOJECT MINI |
OWEN MUMFORD, LTD. |
| K011951 |
06/21/2001 |
EZ SYRINGE |
OWEN MUMFORD, LTD. |
| 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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