| Record ID | K921989 |
|---|---|
| Device Name | FDP - SLIDEX DIRECT |
| Applicant | Biomerieux Vitek, Inc. |
| Product Code | GHH · Hematology |
| Decision Date | Nov 3, 1993 |
| Decision | SESE |
| Submission Type | Traditional |
| Regulation | 21 CFR 864.7320 |
| Device Class | Class 2 |
Predicate graph will load when search results are available.
Embedding visualization will load when search results are available.
PDF viewer will load when search results are available.
Select an item from Submissions
Click any panel, subpart, regulation, product code, or device to see details here.
Loading collections...