HEMOCHRON/FACTOR VI WHOLE BLOOD FACTOR VIII ASSAY
Device Facts
| Record ID | K930235 |
|---|---|
| Device Name | HEMOCHRON/FACTOR VI WHOLE BLOOD FACTOR VIII ASSAY |
| Applicant | Technidyne Corp. |
| Product Code | GGP · Hematology |
| Decision Date | Sep 2, 1993 |
| Decision | SESE |
| Submission Type | Traditional |
| Regulation | 21 CFR 864.7290 |
| Device Class | Class 2 |
