The following data is part of a premarket notification filed by Becton, Dickinson And Company with the FDA for Bd Single Use, Hypodermic Syringe.
| Device ID | K172670 |
| 510k Number | K172670 |
| Device Name: | BD Single Use, Hypodermic Syringe |
| Classification | Syringe, Piston |
| Applicant | Becton, Dickinson And Company 1 Becton Drive Franklin Lakes, NJ 07417 |
| Contact | Victoria Morrow |
| Correspondent | Victoria Morrow Becton, Dickinson And Company 1 Becton Drive Franklin Lakes, NJ 07417 |
| Product Code | FMF |
| CFR Regulation Number | 880.5860 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2017-09-05 |
| Decision Date | 2018-10-23 |
| Summary: | summary |