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 | K151766 |
| 510k Number | K151766 |
| Device Name: | BD Single Use, Hypodermic Syringe |
| Classification | Syringe, Piston |
| Applicant | BECTON, DICKINSON AND COMPANY 1 BECTON DRIVE Franklin Lakes, NJ 07417 |
| Contact | Murtaza Rana |
| Correspondent | Murtaza Rana BECTON, DICKINSON AND COMPANY 1 BECTON DRIVE Franklin Lakes, NJ 07417 |
| Product Code | FMF |
| CFR Regulation Number | 880.5860 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2015-06-30 |
| Decision Date | 2015-09-02 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 50382903033107 | K151766 | 000 |
| 17501073025537 | K151766 | 000 |