The following data is part of a premarket notification filed by Becton Dickinson & Co. with the FDA for Bd L-cath Single And Dual Lument Catheters, Midline Catheter.
| Device ID | K091670 |
| 510k Number | K091670 |
| Device Name: | BD L-CATH SINGLE AND DUAL LUMENT CATHETERS, MIDLINE CATHETER |
| Classification | Catheter, Intravascular, Therapeutic, Long-term Greater Than 30 Days |
| Applicant | BECTON DICKINSON & CO. 9450 SOUTH STATE STREET Sandy, UT 84070 |
| Contact | Justice Alder |
| Correspondent | Justice Alder BECTON DICKINSON & CO. 9450 SOUTH STATE STREET Sandy, UT 84070 |
| Product Code | LJS |
| CFR Regulation Number | 880.5970 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2009-06-09 |
| Decision Date | 2009-07-01 |
| Summary: | summary |