The following data is part of a premarket notification filed by Haemonetics Corporation with the FDA for Automated Blood Cell Separator -filtration.
| Device ID | BK040041 |
| 510k Number | BK040041 |
| Device Name: | Automated Blood Cell Separator -Filtration |
| Classification | Separator, Automated, Blood Cell, Diagnostic |
| Applicant | Haemonetics Corporation 400 Wood Road Braintree, MA 02184 |
| Product Code | GKT |
| CFR Regulation Number | 864.9245 [🔎] |
| Decision | Substantially Equivalent (SE) |
| Type | 510(k) Traditio |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2004-05-14 |
| Decision Date | 2004-07-12 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 30812747013875 | BK040041 | 0 |
| 30812747013851 | BK040041 | 0 |
| 30812747013516 | BK040041 | 0 |