The following data is part of a premarket notification filed by Circle Biologics, Inc. with the FDA for Empty Containers For The Collection & Processing Of Blood/blood Components.
| Device ID | BK100014 |
| 510k Number | BK100014 |
| Device Name: | Empty Containers For The Collection & Processing Of Blood/Blood Components |
| Classification | Container, Empty, For Collection & Processing Of Blood & Blood Components |
| Applicant | Circle Biologics, Inc. 3650 Annapolis Lane, Suite 105 Minneapolis, MN 55447 |
| 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 | 2010-03-01 |
| Decision Date | 2010-07-09 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00817771028870 | BK100014 | 0 |
| 00817771028856 | BK100014 | 0 |
| 00817771028825 | BK100014 | 0 |