The following data is part of a premarket notification filed by Becton, Dickinson & Company with the FDA for Tubes, Vials, Systems, Serum Separators, Blood Collection.
| Device ID | BK210649 |
| 510k Number | BK210649 |
| Device Name: | Tubes, Vials, Systems, Serum Separators, Blood Collection |
| Classification | Tubes, Vials, Systems, Serum Separators, Blood Collection |
| Applicant | Becton, Dickinson & Company 1 Becton Drive Franklin Lakes, NJ 07417 1885 |
| Product Code | JKA |
| CFR Regulation Number | 862.1675 [🔎] |
| Decision | Substantially Equivalent (SE) |
| Type | 510(k) Traditio |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2021-10-25 |
| Decision Date | 2022-01-21 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 50382903648165 | BK210649 | 000 |
| 50382903646062 | BK210649 | 000 |
| 30382903648161 | BK210649 | 000 |
| 30382903646068 | BK210649 | 000 |