The following data is part of a premarket notification filed by Hemo Bioscience with the FDA for Quality Control Kits For Blood Banking Reagents.
| Device ID | BK120022 |
| 510k Number | BK120022 |
| Device Name: | Quality Control Kits For Blood Banking Reagents |
| Classification | Kit, Quality Control For Blood Banking Reagents |
| Applicant | Hemo Bioscience 801 Capitola Drive, Suite 9 research Triangle Park Durham, NC 27713 |
| Product Code | KSF |
| CFR Regulation Number | 864.9650 [🔎] |
| Decision | Substantially Equivalent (SE) |
| Type | 510(k) Traditio |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2012-05-01 |
| Decision Date | 2012-10-24 |