FDA 510(k) Applications Submitted by OWEN MUMFORD, LTD.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K122837 | 09/17/2012 | AUTOJECT 2 FOR GLASSY SYRINGE | OWEN MUMFORD, LTD. |
| K000482 | 02/14/2000 | MODIFICATION TO AUTOJECT MINI | OWEN MUMFORD, LTD. |
| K011951 | 06/21/2001 | EZ SYRINGE | OWEN MUMFORD, LTD. |
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