FDA 510(k) Applications Submitted by JOHN STEPHENS
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K090117 | 01/21/2009 | AUTOSAFE-REFLEX SAFETY HUBER INFUSION SET, AUTOSAFE ADVANTAGE SAFETY HUBER INFUSION SET | AUTOSAFE-REFLEX INC. |
| K071567 | 06/07/2007 | AUTOSAFE-REFLEX SAFETY NEEDLE, AUTOSAFE ADVANTAGE SAFETY NEEDLE | AUTOSAFE-REFELX INC. |
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