Becton, Dickinson and Company · Class II · Cleared May 13, 2011
| K-number | K110771 |
| Device name | BD SINGLE USE, HYPODERMIC SYRINGE |
| Applicant | Becton, Dickinson and Company |
| Product code | FMF |
| Device class | Class II |
| Decision date | May 13, 2011 |
| Decision | Substantially Equivalent |
| Regulation | 880.5860 |
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