The following data is part of a premarket notification filed by Stericon Inc. with the FDA for Empty Containers For The Collection & Processing Of Blood/blood Components.
| Device ID | BK880013 |
| 510k Number | BK880013 |
| Device Name: | Empty Containers For The Collection & Processing Of Blood/Blood Components |
| Classification | Container, Empty, For Collection & Processing Of Blood & Blood Components |
| Applicant | Stericon Inc. 2315 Gardner Road. Broadview, IL 60153 |
| Product Code | KSR |
| CFR Regulation Number | 864.9100 [🔎] |
| Decision | Substantially Equivalent (SE) |
| Type | 510(k) Traditio |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1988-04-22 |
| Decision Date | 1988-11-09 |