BAYER ADVIA 60 HEMATOLOGY SYSTEM (IN VITRO DIAGNOSTIC SYSTEM) — Bayer Corp. (510(k) K982802)
BAYER ADVIA 60 HEMATOLOGY SYSTEM (IN VITRO DIAGNOSTIC SYSTEM) — Bayer Corp. (510(k) K982802) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: BAYER ADVIA 60 HEMATOLOGY SYSTEM (IN VITRO DIAGNOSTIC SYSTEM); Applicant: Bayer Corp.; Clearance track: 510(k).
| Device name | BAYER ADVIA 60 HEMATOLOGY SYSTEM (IN VITRO DIAGNOSTIC SYSTEM) |
|---|---|
| Applicant | Bayer Corp. |
| Clearance track | 510(k) |
| Submission number | K982802 |
| Decision | Substantially Equivalent |
| Decision date | 1998-09-22 |
| Date received | 1998-08-10 |
| Product code | GKZ |
| Device class | 2 |
| Medical specialty | Hematology |
| Applicant location | NY, US |
| Source | openFDA device |
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