The following data is part of a premarket notification filed by Acrometrix Corporation with the FDA for Quality Control Kits For Bloodborne Pathogen Testing Of Donors.
| Device ID | BK040060 |
| 510k Number | BK040060 |
| Device Name: | Quality Control Kits For Bloodborne Pathogen Testing Of Donors |
| Classification | Kit, Test (donors), For Bloodborne Pathogen |
| Applicant | AcroMetrix Corporation 6058 Egret Court Benicia, CA 94510 US |
| Product Code | MYZ |
| CFR Regulation Number | 510(k) Premarket Notification [🔎] |
| Decision | Substantially Equivalent (SE) |
| Type | 510(k) Traditio |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2004-07-07 |
| Decision Date | 2005-05-03 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00884883005945 | BK040060 | 0 |
| 00884883005921 | BK040060 | 0 |
| 00884883005891 | BK040060 | 0 |