Zeus Technologies
FDA 510(k) & PMA Approved Devices — 4 products
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Total Devices4
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K840012 | INDIRECT FLUORESCENT ANTIBODY MYCO | GRZ | 1984-02-27 | View |
| 510(k) | K831026 | INDIRECT FLUORESCENT ANTIBODY REAGENTS | LHL | 1983-06-22 | View |
| 510(k) | K830783 | VERI-STAPH | JWX | 1983-04-08 | View |
| 510(k) | K822859 | DIRECT FA CONJUGATE FOR LEGIONELLA SPP | LHL | 1983-02-16 | View |
No matching devices.
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