The following data is part of a premarket notification filed by Becton, Dickinson & Company with the FDA for Flow Cytometric Reagents And Accessories.
| Device ID | BK210652 |
| 510k Number | BK210652 |
| Device Name: | Flow Cytometric Reagents And Accessories |
| Classification | Flow Cytometric Reagents And Accessories. |
| Applicant | Becton, Dickinson & Company 2350 Qume Dr San Jose, CA 95131 |
| Product Code | OYE |
| CFR Regulation Number | 864.5220 [🔎] |
| Decision | Substantially Equivalent (SE) |
| Type | 510(k) Traditio |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2021-11-05 |
| Decision Date | 2022-01-27 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00382906650061 | BK210652 | 000 |