Becton, Dickinson and Company · Class II · Cleared Jul 16, 2022
| K-number | K213955 |
| Device name | 0.9% Sodium Chloride Injection, USP, BD PosiFlush SafeScrub |
| Applicant | Becton, Dickinson and Company |
| Product code | QTI |
| Device class | Class II |
| Decision date | Jul 16, 2022 |
| Decision | Substantially Equivalent |
| Regulation | — |
AI extraction for this record is queued and will appear within 24 hours. View full FDA record →
View the full FDA submission: accessdata.fda.gov