The following data is part of a premarket notification filed by Becton Dickinson & Co. with the FDA for Bd Careflow Central Venous Catheter.
| Device ID | K033500 |
| 510k Number | K033500 |
| Device Name: | BD CAREFLOW CENTRAL VENOUS CATHETER |
| Classification | Catheter, Intravascular, Therapeutic, Short-term Less Than 30 Days |
| Applicant | BECTON DICKINSON & CO. 9450 SOUTH STATE STREET Sandy, UT 84070 |
| Contact | Leslie Wood |
| Correspondent | Leslie Wood BECTON DICKINSON & CO. 9450 SOUTH STATE STREET Sandy, UT 84070 |
| Product Code | FOZ |
| CFR Regulation Number | 880.5200 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2003-11-05 |
| Decision Date | 2004-01-29 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 20884450321793 | K033500 | 000 |
| 20884450379244 | K033500 | 000 |
| 20884450321892 | K033500 | 000 |
| 20884450321816 | K033500 | 000 |
| 20884450321878 | K033500 | 000 |
| 20884450321908 | K033500 | 000 |
| 20884450321922 | K033500 | 000 |
| 20884450329096 | K033500 | 000 |
| 20884450357884 | K033500 | 000 |
| 20884450321809 | K033500 | 000 |
| 20884450321762 | K033500 | 000 |