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 | K110771 |
510k Number | K110771 |
Device Name: | BD SINGLE USE, HYPODERMIC SYRINGE |
Classification | Syringe, Piston |
Applicant | Becton, Dickinson And Company 1 BECTON DRIVE MC237 Franklin Lakes, NJ 07417 |
Contact | John Roberts |
Correspondent | John Roberts Becton, Dickinson And Company 1 BECTON DRIVE MC237 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 | 2011-03-21 |
Decision Date | 2011-05-13 |
Summary: | summary |