The following data is part of a premarket notification filed by Amtec Diagnostics International Inc. with the FDA for Kit, Quality Control For Blood Banking Reagents.
| Device ID | BK850023 |
| 510k Number | BK850023 |
| Device Name: | Kit, Quality Control For Blood Banking Reagents |
| Classification | Kit, Quality Control For Blood Banking Reagents |
| Applicant | Amtec Diagnostics International Inc. 1107 Ih-45 South Conroe, TX 77305 |
| 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 | 1985-11-14 |
| Decision Date | 1985-12-30 |