The following data is part of a premarket notification filed by Becton, Dickinson, And Company with the FDA for Bd Intelliport System.
| Device ID | K182092 |
| 510k Number | K182092 |
| Device Name: | BD Intelliport System |
| Classification | Infusion Safety Management Software |
| Applicant | Becton, Dickinson, And Company 1 Becton Drive Franklin Lakes, NJ 07417 |
| Contact | Rahul Ram |
| Correspondent | Rahul Ram Becton, Dickinson, And Company 1 Becton Drive Franklin Lakes, NJ 07417 |
| Product Code | PHC |
| CFR Regulation Number | 880.5725 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2018-08-03 |
| Decision Date | 2019-04-30 |